8-42919315-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919315
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919315
    reference: chr 8
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.357A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-96A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.350A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*68A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5383A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*68A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.172A>T
  hgvsp: ENSP00000434430.1:p.Thr58Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.304A>T
  hgvsp: ENSP00000432411.1:p.Thr102Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.229A>T
  hgvsp: ENSP00000435061.1:p.Thr77Ser
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5383A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.377A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5383A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.358A>T
  hgvsp: ENSP00000303423.3:p.Thr120Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-96A>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr120Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

8-42919318-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919318
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919318
    reference: chr 8
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5380C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.361C>T
  hgvsp: ENSP00000303423.3:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.232C>T
  hgvsp: ENSP00000435061.1:p.Arg78Trp
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*71C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.307C>T
  hgvsp: ENSP00000432411.1:p.Arg103Trp
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.175C>T
  hgvsp: ENSP00000434430.1:p.Arg59Trp
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.360C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.380C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.353C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-93C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*71C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-93C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5380C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5380C>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8992
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg121Trp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

8-42919319-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919319
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919319
    reference: chr 8
allele count: 4
allele frequency: 3.29489291598023e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5379G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*72G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.361G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5379G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*72G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5379G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.176G>A
  hgvsp: ENSP00000434430.1:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.381G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.233G>A
  hgvsp: ENSP00000435061.1:p.Arg78Gln
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-92G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.308G>A
  hgvsp: ENSP00000432411.1:p.Arg103Gln
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.362G>A
  hgvsp: ENSP00000303423.3:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-92G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.354G>A
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg121Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

8-42919327-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919327
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919327
    reference: chr 8
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5371A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-84A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*80A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.369A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.362A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.241A>G
  hgvsp: ENSP00000435061.1:p.Ile81Val
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.370A>G
  hgvsp: ENSP00000303423.3:p.Ile124Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*80A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-84A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.184A>G
  hgvsp: ENSP00000434430.1:p.Ile62Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.316A>G
  hgvsp: ENSP00000432411.1:p.Ile106Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.389A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5371A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5371A>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile124Val
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

8-42919340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919340
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919340
    reference: chr 8
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-71C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.402C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-71C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*93C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.382C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*93C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.254C>T
  hgvsp: ENSP00000435061.1:p.Ala85Val
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.383C>T
  hgvsp: ENSP00000303423.3:p.Ala128Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5358C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5358C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.197C>T
  hgvsp: ENSP00000434430.1:p.Ala66Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.375C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.329C>T
  hgvsp: ENSP00000432411.1:p.Ala110Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5358C>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala128Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

8-42919346-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919346
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919346
    reference: chr 8
allele count: 2
allele frequency: 1.648261084555794e-5
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.388A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*99A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.408A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.260A>G
  hgvsp: ENSP00000435061.1:p.Asn87Ser
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.389A>G
  hgvsp: ENSP00000303423.3:p.Asn130Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.203A>G
  hgvsp: ENSP00000434430.1:p.Asn68Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.335A>G
  hgvsp: ENSP00000432411.1:p.Asn112Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5352A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-65A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-65A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*99A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.381A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5352A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5352A>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn130Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-42919380-TATTCCCTGCTTAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919380
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919367
    reference: chr 8
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: TATTCCCTGCTTAA
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

8-42919386-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919386
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919386
    reference: chr 8
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*111+28C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.400+28C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5312C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-53+28C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.347+28C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.393+28C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5312C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.272+28C>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.401+28C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.420+28C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.215+28C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5312C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-53+28C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*111+28C>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8888
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

8-42919387-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919387
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919387
    reference: chr 8
allele count: 1
allele frequency: 8.262687356435807e-6
allele num: 121026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.215+29T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*111+29T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.272+29T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5311T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.401+29T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*111+29T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.400+29T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.420+29T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5311T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-53+29T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.393+29T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5311T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-53+29T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.347+29T>C
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6852
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

8-42919390-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919390
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919390
    reference: chr 8
allele count: 31
allele frequency: 2.562279933215413e-4
allele num: 120986
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.401+32T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*111+32T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5308T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.272+32T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.393+32T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5308T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*111+32T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5308T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-53+32T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.215+32T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.420+32T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-53+32T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.347+32T>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.400+32T>A
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8552
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

8-42919392-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919392
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919392
    reference: chr 8
allele count: 1
allele frequency: 8.265282507356101e-6
allele num: 120988
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.272+34A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*111+34A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-53+34A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.393+34A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-53+34A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.420+34A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.347+34A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5306A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.400+34A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.215+34A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.401+34A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5306A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*111+34A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5306A>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD

8-42919402-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919402
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919402
    reference: chr 8
allele count: 1
allele frequency: 8.296001327360212e-6
allele num: 120540
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5296C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*111+44C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5296C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-53+44C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.215+44C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.420+44C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.401+44C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.272+44C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5296C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.400+44C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-53+44C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*111+44C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.393+44C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.347+44C>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/8-42919405-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42919405
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42919405
    reference: chr 8
allele count: 1
allele frequency: 8.300408380092301e-6
allele num: 120476
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.400+47C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-5293C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.401+47C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-53+47C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*111+47C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.393+47C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.272+47C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-5293C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*111+47C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.347+47C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.420+47C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-5293C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-53+47C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.215+47C>A
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8045
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-42924649-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924649
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924649
    reference: chr 8
allele count: 1
allele frequency: 8.421478137842754e-6
allele num: 118744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.421-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*112-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.401-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.348-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*112-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-52-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.402-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.394-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-52-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.216-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-49G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.273-49G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

8-42924660-GTAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924660
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924657
    reference: chr 8
allele count: 1
allele frequency: 8.402937667008386e-6
allele num: 119006
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-33_201-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.216-33_216-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*112-33_*112-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-33_133-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-52-33_-52-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*112-33_*112-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.421-33_421-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-52-33_-52-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.402-33_402-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.348-33_348-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.394-33_394-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-33_201-31delAAT
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.273-33_273-31delAAT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.401-33_401-31delAAT
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: GTAA
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-42924664-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924664
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924664
    reference: chr 8
allele count: 1
allele frequency: 8.39785686692756e-6
allele num: 119078
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.421-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.401-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*112-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.216-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-52-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.348-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*112-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.402-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-52-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.394-34T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.273-34T>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26780
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD

8-42924665-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924665
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924665
    reference: chr 8
allele count: 3
allele frequency: 2.519272434121026e-5
allele num: 119082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-52-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.348-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-52-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.394-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.402-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.401-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*112-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.216-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*112-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.273-33A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.421-33A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-33A>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

8-42924667-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924667
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924667
    reference: chr 8
allele count: 2
allele frequency: 1.679007370842358e-5
allele num: 119118
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.402-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.401-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*112-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.421-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-52-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.273-31T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.394-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*112-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.348-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-52-31T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.216-31T>C
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26856
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

8-42924669-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924669
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924669
    reference: chr 8
allele count: 6
allele frequency: 5.039560550320012e-5
allele num: 119058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-52-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.394-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.401-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*112-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-52-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.402-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.348-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.421-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.216-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*112-29C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.273-29C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15817
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

8-42924680-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924680
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924680
    reference: chr 8
allele count: 1
allele frequency: 8.350451759440186e-6
allele num: 119754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*112-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-52-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.348-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*112-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.401-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.421-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-52-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.402-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.273-18G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.216-18G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.394-18G>A
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10007
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

8-42924685-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924685
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924685
    reference: chr 8
allele count: 1
allele frequency: 8.333888925928395e-6
allele num: 119992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*112-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.421-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.348-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.402-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.394-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.273-13A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.216-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*112-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-52-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-52-13A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.401-13A>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ

8-42924687-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924687
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924687
    reference: chr 8
allele count: 1
allele frequency: 8.324731111185109e-6
allele num: 120124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*112-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.348-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.421-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.216-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.401-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-52-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.394-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.402-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.273-11G>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*112-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-52-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-11G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-11G>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

8-42924694-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924694
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924694
    reference: chr 8
allele count: 1
allele frequency: 8.297791128001726e-6
allele num: 120514
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.133-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.394-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-52-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.201-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.401-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.201-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.402-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-52-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*112-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.421-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*112-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.216-4C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.273-4C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.348-4C>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.273-4C>T
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

8-42924699-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924699
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924699
    reference: chr 8
allele count: 2
allele frequency: 1.656369569178275e-5
allele num: 120746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.217C>T
  hgvsp: ENSP00000434430.1:p.His73Tyr
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.422C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.395C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.134C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.202C>T
  hgvsp: ENSP00000432892.1:p.His68Tyr
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*113C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.349C>T
  hgvsp: ENSP00000432411.1:p.His117Tyr
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.402C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.274C>T
  hgvsp: ENSP00000435061.1:p.His92Tyr
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.403C>T
  hgvsp: ENSP00000303423.3:p.His135Tyr
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.202C>T
  hgvsp: ENSP00000343931.4:p.His68Tyr
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*113C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His92Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

8-42924704-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924704
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924704
    reference: chr 8
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.279C>T
  hgvsp: ENST00000534420.1:c.279C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*118C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.427C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.139C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.222C>T
  hgvsp: ENST00000533336.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.408C>T
  hgvsp: ENST00000302279.3:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-46C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*118C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.354C>T
  hgvsp: ENST00000531266.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.207C>T
  hgvsp: ENST00000342116.4:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.400C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.407C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.207C>T
  hgvsp: ENST00000533998.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-46C>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Phe93Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-42924722-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924722
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924722
    reference: chr 8
allele count: 2
allele frequency: 1.649294102124291e-5
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.157G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.426G>C
  hgvsp: ENSP00000303423.3:p.Lys142Asn
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.225G>C
  hgvsp: ENSP00000343931.4:p.Lys75Asn
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-28G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.225G>C
  hgvsp: ENSP00000432892.1:p.Lys75Asn
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.240G>C
  hgvsp: ENSP00000434430.1:p.Lys80Asn
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*136G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.372G>C
  hgvsp: ENSP00000432411.1:p.Lys124Asn
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-28G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.445G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.297G>C
  hgvsp: ENSP00000435061.1:p.Lys99Asn
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.418G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*136G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533559
  gene symbol: FNTA
  hgvsc: ENST00000533559.1:n.425G>C
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys99Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

8-42924730-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924730
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924730
    reference: chr 8
allele count: 4
allele frequency: 3.29777235477435e-5
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.453A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.248A>T
  hgvsp: ENSP00000434430.1:p.Gln83Leu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.434A>T
  hgvsp: ENSP00000303423.3:p.Gln145Leu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*144A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.233A>T
  hgvsp: ENSP00000432892.1:p.Gln78Leu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.165A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.426A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-20A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.305A>T
  hgvsp: ENSP00000435061.1:p.Gln102Leu
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.233A>T
  hgvsp: ENSP00000343931.4:p.Gln78Leu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*144A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-20A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.380A>T
  hgvsp: ENSP00000432411.1:p.Gln127Leu
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln145Leu
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

8-42924731-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924731
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924731
    reference: chr 8
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.435G>C
  hgvsp: ENSP00000303423.3:p.Gln145His
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.249G>C
  hgvsp: ENSP00000434430.1:p.Gln83His
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-19G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*145G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-19G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.427G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.234G>C
  hgvsp: ENSP00000432892.1:p.Gln78His
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.166G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*145G>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.306G>C
  hgvsp: ENSP00000435061.1:p.Gln102His
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.381G>C
  hgvsp: ENSP00000432411.1:p.Gln127His
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.234G>C
  hgvsp: ENSP00000343931.4:p.Gln78His
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.454G>C
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln145His
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

8-42924735-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924735
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924735
    reference: chr 8
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.458G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.170G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.310G>A
  hgvsp: ENSP00000435061.1:p.Asp104Asn
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.253G>A
  hgvsp: ENSP00000434430.1:p.Asp85Asn
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.439G>A
  hgvsp: ENSP00000303423.3:p.Asp147Asn
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-15G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.238G>A
  hgvsp: ENSP00000343931.4:p.Asp80Asn
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.238G>A
  hgvsp: ENSP00000432892.1:p.Asp80Asn
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.431G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.385G>A
  hgvsp: ENSP00000432411.1:p.Asp129Asn
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-15G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*149G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*149G>A
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp147Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-42924738-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924738
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924738
    reference: chr 8
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.434C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.256C>A
  hgvsp: ENSP00000434430.1:p.Leu86Ile
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*152C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.442C>A
  hgvsp: ENSP00000303423.3:p.Leu148Ile
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.173C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.388C>A
  hgvsp: ENSP00000432411.1:p.Leu130Ile
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.241C>A
  hgvsp: ENSP00000432892.1:p.Leu81Ile
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*152C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.461C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.241C>A
  hgvsp: ENSP00000343931.4:p.Leu81Ile
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.313C>A
  hgvsp: ENSP00000435061.1:p.Leu105Ile
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu148Ile
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-42924742-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924742
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924742
    reference: chr 8
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.465A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.260A>G
  hgvsp: ENSP00000434430.1:p.His87Arg
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.438A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.446A>G
  hgvsp: ENSP00000303423.3:p.His149Arg
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.245A>G
  hgvsp: ENSP00000343931.4:p.His82Arg
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.392A>G
  hgvsp: ENSP00000432411.1:p.His131Arg
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.177A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.317A>G
  hgvsp: ENSP00000435061.1:p.His106Arg
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.-8A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.245A>G
  hgvsp: ENSP00000432892.1:p.His82Arg
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.-8A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*156A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*156A>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His149Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

8-42924758-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924758
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924758
    reference: chr 8
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.276C>T
  hgvsp: ENST00000533336.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.408C>T
  hgvsp: ENST00000531266.1:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.261C>T
  hgvsp: ENST00000533998.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.481C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.333C>T
  hgvsp: ENST00000534420.1:c.333C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.9C>T
  hgvsp: ENST00000529687.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.193C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.462C>T
  hgvsp: ENST00000302279.3:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.261C>T
  hgvsp: ENST00000342116.4:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*172C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.9C>T
  hgvsp: ENST00000525699.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.454C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*172C>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10122
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr154Tyr
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

8-42924767-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924767
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924767
    reference: chr 8
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.18A>G
  hgvsp: ENST00000529687.1:c.18A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*181A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*181A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.342A>G
  hgvsp: ENST00000534420.1:c.342A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.202A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.471A>G
  hgvsp: ENST00000302279.3:c.471A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.18A>G
  hgvsp: ENST00000525699.1:c.18A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.270A>G
  hgvsp: ENST00000342116.4:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.285A>G
  hgvsp: ENST00000533336.1:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.417A>G
  hgvsp: ENST00000531266.1:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.270A>G
  hgvsp: ENST00000533998.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.490A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.463A>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28101
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala157Ala
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum

8-42924768-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924768
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924768
    reference: chr 8
allele count: 1
allele frequency: 8.273625337150233e-6
allele num: 120866
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.343A>G
  hgvsp: ENSP00000435061.1:p.Ile115Val
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.472A>G
  hgvsp: ENSP00000303423.3:p.Ile158Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.203A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.286A>G
  hgvsp: ENSP00000434430.1:p.Ile96Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.271A>G
  hgvsp: ENSP00000432892.1:p.Ile91Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.19A>G
  hgvsp: ENSP00000436998.1:p.Ile7Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*182A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.19A>G
  hgvsp: ENSP00000473479.1:p.Ile7Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.464A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*182A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.418A>G
  hgvsp: ENSP00000432411.1:p.Ile140Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.491A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.271A>G
  hgvsp: ENSP00000343931.4:p.Ile91Val
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10090
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile158Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-42924784-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924784
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924784
    reference: chr 8
allele count: 1
allele frequency: 8.38208915190022e-6
allele num: 119302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.287C>A
  hgvsp: ENSP00000432892.1:p.Pro96His
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.488C>A
  hgvsp: ENSP00000303423.3:p.Pro163His
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.302C>A
  hgvsp: ENSP00000434430.1:p.Pro101His
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.359C>A
  hgvsp: ENSP00000435061.1:p.Pro120His
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.480C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.434C>A
  hgvsp: ENSP00000432411.1:p.Pro145His
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.507C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.219C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.287C>A
  hgvsp: ENSP00000343931.4:p.Pro96His
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.35C>A
  hgvsp: ENSP00000436998.1:p.Pro12His
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*198C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*198C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.35C>A
  hgvsp: ENSP00000473479.1:p.Pro12His
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27081
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro163His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

8-42924794-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924794
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924794
    reference: chr 8
allele count: 1
allele frequency: 8.590770076629668e-6
allele num: 116404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.297T>C
  hgvsp: ENST00000533998.1:c.297T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.312T>C
  hgvsp: ENST00000533336.1:c.312T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.297T>C
  hgvsp: ENST00000342116.4:c.297T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.498T>C
  hgvsp: ENST00000302279.3:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.517T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*208T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.369T>C
  hgvsp: ENST00000534420.1:c.369T>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.444T>C
  hgvsp: ENST00000531266.1:c.444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.45T>C
  hgvsp: ENST00000529687.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*208T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.229T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.45T>C
  hgvsp: ENST00000525699.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.490T>C
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr166Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-42924797-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924797
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924797
    reference: chr 8
allele count: 9
allele frequency: 7.9175170666479e-5
allele num: 113672
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.48A>G
  hgvsp: ENST00000529687.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.520A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.300A>G
  hgvsp: ENST00000533998.1:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.232A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.48A>G
  hgvsp: ENST00000525699.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.447A>G
  hgvsp: ENST00000531266.1:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*211A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.501A>G
  hgvsp: ENST00000302279.3:c.501A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.315A>G
  hgvsp: ENST00000533336.1:c.315A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.493A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.300A>G
  hgvsp: ENST00000342116.4:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*211A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.372A>G
  hgvsp: ENST00000534420.1:c.372A>G(p.%3D)
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13528
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7070
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln167Gln
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP

8-42924810-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924810
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924810
    reference: chr 8
allele count: 2
allele frequency: 1.800568979797616e-5
allele num: 111076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+8T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.53+8T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.320+8T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.53+8T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.305+8T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*216+8T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.506+8T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.498+8T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*216+8T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.452+8T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.377+8T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.237+8T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+8T>C
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17212
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.377+8T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum

8-42924813-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924813
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924813
    reference: chr 8
allele count: 1
allele frequency: 9.075068970524176e-6
allele num: 110192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.320+11A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+11A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.53+11A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*216+11A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.452+11A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.53+11A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*216+11A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.506+11A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.305+11A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.237+11A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.498+11A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.377+11A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+11A>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD

8-42924819-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924819
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924819
    reference: chr 8
allele count: 1
allele frequency: 9.231394125140779e-6
allele num: 108326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+17G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.506+17G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.53+17G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*216+17G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.320+17G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.452+17G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+17G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*216+17G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.305+17G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.53+17G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.377+17G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.237+17G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.498+17G>A
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12219
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD

8-42924820-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924820
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924820
    reference: chr 8
allele count: 1
allele frequency: 9.251549634563789e-6
allele num: 108090
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*216+18C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.53+18C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.498+18C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.305+18C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+18C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.237+18C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.377+18C>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*216+18C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.53+18C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+18C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.506+18C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.452+18C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.320+18C>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11109
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

8-42924821-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924821
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924821
    reference: chr 8
allele count: 1
allele frequency: 9.248127254231018e-6
allele num: 108130
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.53+19T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.305+19T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*216+19T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.498+19T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*216+19T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.53+19T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+19T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.506+19T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+19T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.452+19T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.320+19T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.377+19T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.237+19T>C
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19055
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11336
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

8-42924823-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924823
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924823
    reference: chr 8
allele count: 1
allele frequency: 9.285223495329533e-6
allele num: 107698
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.377+21T>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.506+21T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.237+21T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+21T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.53+21T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+21T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*216+21T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.498+21T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.452+21T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.320+21T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*216+21T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.53+21T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.305+21T>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8199
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

8-42924828-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924828
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924828
    reference: chr 8
allele count: 10
allele frequency: 9.437701730874498e-5
allele num: 105958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*216+26C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.498+26C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.377+26C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.305+26C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*216+26C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.320+26C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+26C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+26C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.53+26C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.237+26C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.53+26C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.506+26C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.452+26C>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21885
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6545
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9776
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8695
  bin: 2.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-42924831-AGGCTGGAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924831
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924823
    reference: chr 8
allele count: 1
allele frequency: 9.495053077346703e-6
allele num: 105318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6878
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10880
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7004
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: AGGCTGGAG
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

8-42924833-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924833
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924833
    reference: chr 8
allele count: 3
allele frequency: 2.873948613798785e-5
allele num: 104386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.498+31G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.320+31G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.305+31G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+31G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*216+31G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.506+31G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.377+31G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.237+31G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+31G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.53+31G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.452+31G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.53+31G>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*216+31G>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7310
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11648
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-42924844-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42924844
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42924844
    reference: chr 8
allele count: 5
allele frequency: 5.009819245721615e-5
allele num: 99804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.53+42G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+42G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.377+42G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*216+42G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.452+42G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.305+42G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*216+42G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.506+42G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.53+42G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.237+42G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.320+42G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+42G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000524546
  gene symbol: FNTA
  hgvsc: ENST00000524546.1:n.498+42G>A
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15254
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22177
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

8-42927277-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927277
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927277
    reference: chr 8
allele count: 1
allele frequency: 8.88320363856021e-6
allele num: 112572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*217-47T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*217-47T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.507-47T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2475T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.453-47T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.306-47T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2475T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.54-47T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.378-47T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.54-47T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.238-47T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.321-47T>C
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16068
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

8-42927298-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927298
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927298
    reference: chr 8
allele count: 1
allele frequency: 8.82861885086697e-6
allele num: 113268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.321-26A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*217-26A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.507-26A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*217-26A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.54-26A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2496A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.306-26A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2496A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.54-26A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.453-26A>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.378-26A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.238-26A>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

8-42927302-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927302
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927302
    reference: chr 8
allele count: 2
allele frequency: 1.762362976278594e-5
allele num: 113484
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.378-22C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.54-22C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2500C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.54-22C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.238-22C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.453-22C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2500C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.321-22C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*217-22C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.306-22C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.507-22C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*217-22C>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/8-42927306-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927306
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927306
    reference: chr 8
allele count: 1
allele frequency: 8.772545441785388e-6
allele num: 113992
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*217-18C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*217-18C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.507-18C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.306-18C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2504C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2504C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.54-18C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.453-18C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.54-18C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.238-18C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.321-18C>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.378-18C>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

8-42927307-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927307
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927307
    reference: chr 8
allele count: 2
allele frequency: 1.751773670841727e-5
allele num: 114170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.321-17C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.54-17C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.453-17C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*217-17C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.378-17C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2505C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.507-17C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.54-17C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.238-17C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2505C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.306-17C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*217-17C>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

8-42927320-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927320
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927320
    reference: chr 8
allele count: 1
allele frequency: 8.602890571231935e-6
allele num: 116240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.54-4T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.54-4T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2518T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.321-4T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*217-4T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.453-4T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*217-4T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.306-4T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2518T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.378-4T>G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.507-4T>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.238-4T>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16075
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.378-4T>G
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: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

8-42927321-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927321
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927321
    reference: chr 8
allele count: 1
allele frequency: 8.594018563080097e-6
allele num: 116360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.54-3T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.238-3T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*217-3T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.378-3T>C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.321-3T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.54-3T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*217-3T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.306-3T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2519T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.453-3T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.507-3T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2519T>C
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.378-3T>C
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

8-42927335-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927335
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927335
    reference: chr 8
allele count: 1
allele frequency: 8.434263351438885e-6
allele num: 118564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.317G>A
  hgvsp: ENSP00000343931.4:p.Arg106Gln
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.518G>A
  hgvsp: ENSP00000303423.3:p.Arg173Gln
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*228G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.65G>A
  hgvsp: ENSP00000436998.1:p.Arg22Gln
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.389G>A
  hgvsp: ENSP00000435061.1:p.Arg130Gln
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.332G>A
  hgvsp: ENSP00000434430.1:p.Arg111Gln
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2533G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*228G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.65G>A
  hgvsp: ENSP00000473479.1:p.Arg22Gln
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2533G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.249G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.464G>A
  hgvsp: ENSP00000432411.1:p.Arg155Gln
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg130Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

8-42927337-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927337
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927337
    reference: chr 8
allele count: 1
allele frequency: 8.411560849231184e-6
allele num: 118884
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.391G>A
  hgvsp: ENSP00000435061.1:p.Val131Ile
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2535G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.466G>A
  hgvsp: ENSP00000432411.1:p.Val156Ile
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.319G>A
  hgvsp: ENSP00000343931.4:p.Val107Ile
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.67G>A
  hgvsp: ENSP00000473479.1:p.Val23Ile
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.67G>A
  hgvsp: ENSP00000436998.1:p.Val23Ile
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*230G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.334G>A
  hgvsp: ENSP00000434430.1:p.Val112Ile
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.520G>A
  hgvsp: ENSP00000303423.3:p.Val174Ile
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.251G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*230G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2535G>A
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val131Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

8-42927345-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927345
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927345
    reference: chr 8
allele count: 1
allele frequency: 8.361903169161301e-6
allele num: 119590
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.528G>A
  hgvsp: ENST00000302279.3:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2543G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.342G>A
  hgvsp: ENST00000533336.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*238G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*238G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.75G>A
  hgvsp: ENST00000529687.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2543G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.75G>A
  hgvsp: ENST00000525699.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.399G>A
  hgvsp: ENST00000534420.1:c.399G>A(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.327G>A
  hgvsp: ENST00000342116.4:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.259G>A
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.474G>A
  hgvsp: ENST00000531266.1:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val133Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

8-42927354-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927354
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927354
    reference: chr 8
allele count: 5
allele frequency: 4.157520122397393e-5
allele num: 120264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.351A>G
  hgvsp: ENST00000533336.1:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2552A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*247A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.408A>G
  hgvsp: ENST00000534420.1:c.408A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*247A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.336A>G
  hgvsp: ENST00000342116.4:c.336A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2552A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.84A>G
  hgvsp: ENST00000529687.1:c.84A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.483A>G
  hgvsp: ENST00000531266.1:c.483A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.268A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.84A>G
  hgvsp: ENST00000525699.1:c.84A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.537A>G
  hgvsp: ENST00000302279.3:c.537A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11652
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu136Leu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

8-42927361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927361
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927361
    reference: chr 8
allele count: 1
allele frequency: 8.289811821271656e-6
allele num: 120630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*254C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.91C>T
  hgvsp: ENSP00000473479.1:p.Pro31Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.91C>T
  hgvsp: ENSP00000436998.1:p.Pro31Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.544C>T
  hgvsp: ENSP00000303423.3:p.Pro182Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.358C>T
  hgvsp: ENSP00000434430.1:p.Pro120Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.343C>T
  hgvsp: ENSP00000343931.4:p.Pro115Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.490C>T
  hgvsp: ENSP00000432411.1:p.Pro164Ser
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2559C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.275C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2559C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.415C>T
  hgvsp: ENSP00000435061.1:p.Pro139Ser
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*254C>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro139Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-42927362-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927362
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927362
    reference: chr 8
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2560C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.545C>T
  hgvsp: ENSP00000303423.3:p.Pro182Leu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.416C>T
  hgvsp: ENSP00000435061.1:p.Pro139Leu
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.92C>T
  hgvsp: ENSP00000473479.1:p.Pro31Leu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.359C>T
  hgvsp: ENSP00000434430.1:p.Pro120Leu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*255C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.92C>T
  hgvsp: ENSP00000436998.1:p.Pro31Leu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.491C>T
  hgvsp: ENSP00000432411.1:p.Pro164Leu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.344C>T
  hgvsp: ENSP00000343931.4:p.Pro115Leu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*255C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2560C>T
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.276C>T
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro139Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-42927368-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927368
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927368
    reference: chr 8
allele count: 1
allele frequency: 8.279790686891435e-6
allele num: 120776
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.422A>G
  hgvsp: ENSP00000435061.1:p.Gln141Arg
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.551A>G
  hgvsp: ENSP00000303423.3:p.Gln184Arg
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.350A>G
  hgvsp: ENSP00000343931.4:p.Gln117Arg
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.497A>G
  hgvsp: ENSP00000432411.1:p.Gln166Arg
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*261A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.98A>G
  hgvsp: ENSP00000436998.1:p.Gln33Arg
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.365A>G
  hgvsp: ENSP00000434430.1:p.Gln122Arg
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.98A>G
  hgvsp: ENSP00000473479.1:p.Gln33Arg
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*261A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.282A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2566A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2566A>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln141Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-42927382-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927382
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927382
    reference: chr 8
allele count: 1
allele frequency: 8.275953389830508e-6
allele num: 120832
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2580A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.379A>G
  hgvsp: ENSP00000434430.1:p.Ile127Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.112A>G
  hgvsp: ENSP00000473479.1:p.Ile38Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.112A>G
  hgvsp: ENSP00000436998.1:p.Ile38Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.296A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2580A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*275A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.436A>G
  hgvsp: ENSP00000435061.1:p.Ile146Val
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.511A>G
  hgvsp: ENSP00000432411.1:p.Ile171Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.565A>G
  hgvsp: ENSP00000303423.3:p.Ile189Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.364A>G
  hgvsp: ENSP00000343931.4:p.Ile122Val
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*275A>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile146Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-42927389-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927389
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927389
    reference: chr 8
allele count: 2
allele frequency: 1.655492095025246e-5
allele num: 120810
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2587A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.443A>G
  hgvsp: ENSP00000435061.1:p.Asp148Gly
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*282A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.119A>G
  hgvsp: ENSP00000436998.1:p.Asp40Gly
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.371A>G
  hgvsp: ENSP00000343931.4:p.Asp124Gly
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*282A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2587A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.386A>G
  hgvsp: ENSP00000434430.1:p.Asp129Gly
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.518A>G
  hgvsp: ENSP00000432411.1:p.Asp173Gly
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.119A>G
  hgvsp: ENSP00000473479.1:p.Asp40Gly
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.572A>G
  hgvsp: ENSP00000303423.3:p.Asp191Gly
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.303A>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6251
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp148Gly
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

8-42927392-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927392
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927392
    reference: chr 8
allele count: 3
allele frequency: 2.483443708609272e-5
allele num: 120800
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*285T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.306T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*285T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.374T>C
  hgvsp: ENSP00000343931.4:p.Ile125Thr
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.389T>C
  hgvsp: ENSP00000434430.1:p.Ile130Thr
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.575T>C
  hgvsp: ENSP00000303423.3:p.Ile192Thr
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.122T>C
  hgvsp: ENSP00000436998.1:p.Ile41Thr
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2590T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.521T>C
  hgvsp: ENSP00000432411.1:p.Ile174Thr
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2590T>C
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.446T>C
  hgvsp: ENSP00000435061.1:p.Ile149Thr
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.122T>C
  hgvsp: ENSP00000473479.1:p.Ile41Thr
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile149Thr
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

8-42927407-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927407
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927407
    reference: chr 8
allele count: 1
allele frequency: 8.285004142502071e-6
allele num: 120700
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.389C>G
  hgvsp: ENSP00000343931.4:p.Ala130Gly
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.137C>G
  hgvsp: ENSP00000436998.1:p.Ala46Gly
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2605C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.461C>G
  hgvsp: ENSP00000435061.1:p.Ala154Gly
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.590C>G
  hgvsp: ENSP00000303423.3:p.Ala197Gly
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.536C>G
  hgvsp: ENSP00000432411.1:p.Ala179Gly
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*300C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2605C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.404C>G
  hgvsp: ENSP00000434430.1:p.Ala135Gly
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*300C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.321C>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.137C>G
  hgvsp: ENSP00000473479.1:p.Ala46Gly
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala154Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

8-42927409-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42927409
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42927409
    reference: chr 8
allele count: 1
allele frequency: 8.287063893262618e-6
allele num: 120670
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000434430
  ensembl transcript: ENST00000533336
  gene symbol: FNTA
  hgvsc: ENST00000533336.1:c.406A>G
  hgvsp: ENSP00000434430.1:p.Lys136Glu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000436998
  ensembl transcript: ENST00000525699
  gene symbol: FNTA
  hgvsc: ENST00000525699.1:c.139A>G
  hgvsp: ENSP00000436998.1:p.Lys47Glu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000533368
  gene symbol: FNTA
  hgvsc: ENST00000533368.1:n.323A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432892
  ensembl transcript: ENST00000533998
  gene symbol: FNTA
  hgvsc: ENST00000533998.1:c.305+2607A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000303423
  ensembl transcript: ENST00000302279
  gene symbol: FNTA
  hgvsc: ENST00000302279.3:c.592A>G
  hgvsp: ENSP00000303423.3:p.Lys198Glu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000343931
  ensembl transcript: ENST00000342116
  gene symbol: FNTA
  hgvsc: ENST00000342116.4:c.391A>G
  hgvsp: ENSP00000343931.4:p.Lys131Glu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000432411
  ensembl transcript: ENST00000531266
  gene symbol: FNTA
  hgvsc: ENST00000531266.1:c.538A>G
  hgvsp: ENSP00000432411.1:p.Lys180Glu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254673
  ensembl protein: ENSP00000435061
  ensembl transcript: ENST00000534420
  gene symbol: RP11-598P20.5
  hgvsc: ENST00000534420.1:c.463A>G
  hgvsp: ENSP00000435061.1:p.Lys155Glu
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000435455
  ensembl transcript: ENST00000533383
  gene symbol: FNTA
  hgvsc: ENST00000533383.1:c.*302A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000473479
  ensembl transcript: ENST00000529687
  gene symbol: FNTA
  hgvsc: ENST00000529687.1:c.139A>G
  hgvsp: ENSP00000473479.1:p.Lys47Glu
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168522
  ensembl transcript: ENST00000527153
  gene symbol: FNTA
  hgvsc: ENST00000527153.1:n.525+2607A>G
  variant of: http://identifiers.org/hgnc/3782
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168522
  ensembl protein: ENSP00000437208
  ensembl transcript: ENST00000526755
  gene symbol: FNTA
  hgvsc: ENST00000526755.1:c.*302A>G
  variant of: http://identifiers.org/hgnc/3782
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11753
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys155Glu
num of homozygotes: 0
reference allele: A

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

GenotypeDepth
all individuals: 1259
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6853
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8146
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8998
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3637
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 13571
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2330
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4577
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27640
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: -1.044e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 4.812e0

DP
type: SiteQuality
SIO_000300: 2.543724e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

QD
type: SiteQuality
SIO_000300: 1.087e1

GenotypeDepth
all individuals: 597
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 861
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8146
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2556
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 3545
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3337
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4578
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13571
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3637
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2329
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 27644
bin: 9.75e1
variant carriers: 4

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

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

GenotypeQuality
all individuals: 2043
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.927e1

QD
type: SiteQuality
SIO_000300: 9.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.97e-1

FS
type: SiteQuality
SIO_000300: 2.551e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

MQRankSum
type: SiteQuality
SIO_000300: -4.81e-1

DP
type: SiteQuality
SIO_000300: 2.544069e6

VQSLOD
type: SiteQuality
SIO_000300: 1.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

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

GenotypeDepth
all individuals: 3363
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8993
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 861
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9104
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2051
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4580
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3545
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3337
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13570
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3637
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 27642
bin: 9.75e1
variant carriers: 4

Latino
type: Population
allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.543983e6

QD
type: SiteQuality
SIO_000300: 1.21e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.49e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeDepth
all individuals: 1259
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8146
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6856
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10189
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8994
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2051
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3634
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2327
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3545
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4582
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13564
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3337
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2044
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27639
bin: 9.75e1
variant carriers: 1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.195e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.35e0

DP
type: SiteQuality
SIO_000300: 2.54342e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

VQSLOD
type: SiteQuality
SIO_000300: -3.474e0

QD
type: SiteQuality
SIO_000300: 1.396e1

FS
type: SiteQuality
SIO_000300: 1.6342e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.89e-1

MQ
type: SiteQuality
SIO_000300: 5.993e1

GenotypeDepth
all individuals: 338
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2551
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10158
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1260
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3364
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8145
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 27639
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3543
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13526
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4576
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3635
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2326
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3336
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.009e1

VQSLOD
type: SiteQuality
SIO_000300: -1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.722e0

FS
type: SiteQuality
SIO_000300: 3.675e0

DP
type: SiteQuality
SIO_000300: 2.54305e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

MQ
type: SiteQuality
SIO_000300: 5.843e1

GenotypeDepth
all individuals: 9093
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2552
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5142
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8989
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2043
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27639
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3540
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13492
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4583
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2323
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3336
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3629
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.53e0

MQRankSum
type: SiteQuality
SIO_000300: 1.66e-1

DP
type: SiteQuality
SIO_000300: 2.542598e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-2

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.385e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

GenotypeDepth
all individuals: 8137
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2551
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 202
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2293
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27639
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12175
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2040
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3592
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4465
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.031e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

MQ
type: SiteQuality
SIO_000300: 4.88e1

DP
type: SiteQuality
SIO_000300: 2.529623e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 3.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQRankSum
type: SiteQuality
SIO_000300: -7.423e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.74e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.696e-1

GenotypeDepth
all individuals: 2052
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5146
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3364
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8720
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 260
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3577
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11788
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3330
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27638
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4426
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 3.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.646e1

DP
type: SiteQuality
SIO_000300: 2.525876e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.392e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.000000000000001e-2

FS
type: SiteQuality
SIO_000300: 3.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-1

GenotypeDepth
all individuals: 8132
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 597
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8670
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3362
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1260
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8858
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3330
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 290
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4426
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2037
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27642
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11620
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3576
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502268425322237e-5
allele num: 66566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.307e1

MQRankSum
type: SiteQuality
SIO_000300: 6.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.064e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.524033e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

FS
type: SiteQuality
SIO_000300: 3.01e0

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.01e-1

GenotypeDepth
all individuals: 2053
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 8809
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 597
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 408
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5144
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 330
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 433
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3563
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4350
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2262
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11189
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2036
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3517
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27661
bin: 9.75e1
variant carriers: 31

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.40442414041837e-4
allele num: 66544
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.659969088098918e-5
allele num: 10352
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.539709649871904e-4
allele num: 16394
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

QD
type: SiteQuality
SIO_000300: 1.402e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.17e0

MQ
type: SiteQuality
SIO_000300: 5.991e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.67e0

DP
type: SiteQuality
SIO_000300: 2.520395e6

GenotypeDepth
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6849
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 598
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2054
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 408
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1122
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27645
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2036
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11337
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3562
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3330
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 531
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2264
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3517
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502674761074713e-5
allele num: 66548
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.239e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.94e-1

FS
type: SiteQuality
SIO_000300: 5.9284e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.98e-1

MQ
type: SiteQuality
SIO_000300: 3.689e1

DP
type: SiteQuality
SIO_000300: 2.519934e6

VQSLOD
type: SiteQuality
SIO_000300: -5.1e0

QD
type: SiteQuality
SIO_000300: 2.6e0

GenotypeDepth
all individuals: 493
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 330
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 597
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2056
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1261
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2551
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3328
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27641
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 509
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3859
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3481
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7680
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16324
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.435e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

DP
type: SiteQuality
SIO_000300: 2.504235e6

VQSLOD
type: SiteQuality
SIO_000300: 4.62e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.343e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 7952
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1132
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1260
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2551
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7897
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3477
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1309
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3852
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27641
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 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: 8586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16290
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.667013347200555e-5
allele num: 11538
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 2.504093e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.38e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3219
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13014
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8753
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1174
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34967
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2389
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 383
bin: 5.75e1
variant carriers: 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: 1
allele frequency: 1.516208266367468e-5
allele num: 65954
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14768
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.885e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

QD
type: SiteQuality
SIO_000300: 1.395e1

DP
type: SiteQuality
SIO_000300: 1.635754e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

GenotypeDepth
all individuals: 229
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2483
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9943
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37990
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2271
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8782
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14934
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66028
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

QD
type: SiteQuality
SIO_000300: 1.075e1

FS
type: SiteQuality
SIO_000300: 2.612e0

VQSLOD
type: SiteQuality
SIO_000300: 2.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.22e-1

DP
type: SiteQuality
SIO_000300: 1.649095e6

MQ
type: SiteQuality
SIO_000300: 5.752e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

GenotypeDepth
all individuals: 997
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2274
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1102
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2374
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 860
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2270
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8822
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38713
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 4.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.677350427350428e-5
allele num: 14976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66050
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: 888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 1.654007e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 5.342e0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

QD
type: SiteQuality
SIO_000300: 9.82e0

GenotypeDepth
all individuals: 1789
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9945
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2374
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38995
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8833
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2271
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 923
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66050
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.891844997108155e-4
allele num: 10374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.554e1

FS
type: SiteQuality
SIO_000300: 1.214e0

VQSLOD
type: SiteQuality
SIO_000300: 8.81e-1

DP
type: SiteQuality
SIO_000300: 1.655484e6

MQ
type: SiteQuality
SIO_000300: 5.919e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e0

MQRankSum
type: SiteQuality
SIO_000300: -7.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
all individuals: 139
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1086
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15664
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 587
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 261
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2372
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 39281
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2237
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 879
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 923
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8837
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2275
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15010
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.027825718351652e-5
allele num: 66054
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

FS
type: SiteQuality
SIO_000300: 1.486e0

DP
type: SiteQuality
SIO_000300: 1.657906e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.32e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.229e1

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 261
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9989
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39437
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1160
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2267
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8823
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 644
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 9.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 14964
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.645061728395061e-5
allele num: 10368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.542288707870272e-5
allele num: 66046
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 1.662023e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.054e1

FS
type: SiteQuality
SIO_000300: 7.003e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.593e0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 228
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 966
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41054
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 322
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8960
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2239
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15456
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: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510163399679845e-5
allele num: 66218
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.677828e6

VQSLOD
type: SiteQuality
SIO_000300: -2.423e0

MQ
type: SiteQuality
SIO_000300: 5.799e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: 3.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 3.762e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.844e0

QD
type: SiteQuality
SIO_000300: 7.96e0

GenotypeDepth
all individuals: 27387
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17329
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41408
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2303
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 199
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8985
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2365
bin: 9.75e1
variant carriers: 1

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: 10392
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15608
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.682739e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.486e0

VQSLOD
type: SiteQuality
SIO_000300: -1.244e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.521e0

FS
type: SiteQuality
SIO_000300: 3.998e0

QD
type: SiteQuality
SIO_000300: 1.21e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

MQ
type: SiteQuality
SIO_000300: 5.929e1

GenotypeDepth
all individuals: 177
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17471
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 137
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2242
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 204
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41558
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 302
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9002
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2364
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 92
bin: 4.75e1
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: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15702
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66328
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.558e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.064e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.29e1

DP
type: SiteQuality
SIO_000300: 1.684877e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

FS
type: SiteQuality
SIO_000300: 6.808e0

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

GenotypeDepth
all individuals: 284
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 228
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 260
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1792
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 494
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 181
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2363
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66440
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.069e0

DP
type: SiteQuality
SIO_000300: 1.69228e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.521e0

MQ
type: SiteQuality
SIO_000300: 5.763e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

FS
type: SiteQuality
SIO_000300: 7.163e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.516e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.649e0

GenotypeDepth
all individuals: 249
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10101
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 227
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 588
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 260
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2249
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2363
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2321
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9064
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42273
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007880647295915e-5
allele num: 66492
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16146
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.488e0

QD
type: SiteQuality
SIO_000300: 2.504e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.656e0

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.136e0

DP
type: SiteQuality
SIO_000300: 1.696959e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.858e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

GenotypeDepth
all individuals: 356
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1796
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 227
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 930
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9105
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2361
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 302
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42516
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66546
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.699698e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.955e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.02e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 3.183e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.73e0

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10123
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 260
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42874
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2343
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2262
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2361
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 302
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.213444970270598e-4
allele num: 16482
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.432e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.4e-1

QD
type: SiteQuality
SIO_000300: 9.65e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.227e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.704818e6

GenotypeDepth
all individuals: 356
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 227
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2363
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 86
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42892
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 302
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2340
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2259
bin: 7.75e1
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: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.425418384671356e-4
allele num: 16492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: 4.3e-1

QD
type: SiteQuality
SIO_000300: 1.16e1

DP
type: SiteQuality
SIO_000300: 1.705188e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.075e0

MQRankSum
type: SiteQuality
SIO_000300: -4.48e-1

FS
type: SiteQuality
SIO_000300: 1.003e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.66e-1

GenotypeDepth
all individuals: 136
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28149
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 227
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 302
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42904
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2340
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9176
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2258
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.705212e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

FS
type: SiteQuality
SIO_000300: 1.86e0

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 6.35e-1

GenotypeDepth
all individuals: 1795
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 89
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2358
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2343
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2257
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42884
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.705191e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.13e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.541e0

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17993
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 178
bin: 6.25e1
variant carriers: 1

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

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

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

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

GenotypeQuality
all individuals: 42894
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9175
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2358
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2253
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -7.01e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.047e0

FS
type: SiteQuality
SIO_000300: 5.06e0

MQ
type: SiteQuality
SIO_000300: 5.914e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.79e-1

DP
type: SiteQuality
SIO_000300: 1.705239e6

QD
type: SiteQuality
SIO_000300: 1.118e1

GenotypeDepth
all individuals: 53
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42856
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2357
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2342
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9169
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 929
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
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: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.148e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.511e0

VQSLOD
type: SiteQuality
SIO_000300: -1.436e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.56e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

DP
type: SiteQuality
SIO_000300: 1.704792e6

GenotypeDepth
all individuals: 136
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 226
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1788
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 215
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2357
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42747
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.512e0

FS
type: SiteQuality
SIO_000300: 3.419e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.391e0

QD
type: SiteQuality
SIO_000300: 4.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.94e-1

DP
type: SiteQuality
SIO_000300: 1.70308e6

MQ
type: SiteQuality
SIO_000300: 5.873e1

GenotypeDepth
all individuals: 366
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 226
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 587
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2355
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42427
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 910
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9089
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.711e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

DP
type: SiteQuality
SIO_000300: 1.698258e6

QD
type: SiteQuality
SIO_000300: 9.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.47e-1

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 226
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1779
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2355
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2228
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9075
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42227
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504936190705514e-5
allele num: 66448
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.16e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-1

DP
type: SiteQuality
SIO_000300: 1.696359e6

VQSLOD
type: SiteQuality
SIO_000300: 6.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

FS
type: SiteQuality
SIO_000300: 3.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 136
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 579
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 402
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40101
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2213
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8780
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2097
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2205
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2335
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.171783454417624e-4
allele num: 8534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65514
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.014e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.32e-1

QD
type: SiteQuality
SIO_000300: 1.309e1

VQSLOD
type: SiteQuality
SIO_000300: 7.07e-1

DP
type: SiteQuality
SIO_000300: 1.661975e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.087e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1668
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 227
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35493
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1174
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2321
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1954
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5558
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2036
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567250728771589e-5
allele num: 63806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11078
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.582546e6

MQRankSum
type: SiteQuality
SIO_000300: 8.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.188e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.1e-2

QD
type: SiteQuality
SIO_000300: 1.745e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-1

GenotypeDepth
all individuals: 336
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 21892
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 226
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 136
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1772
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 480
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9126
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31005
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5077
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 9
allele frequency: 9.168704156479218e-4
allele num: 9816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15742
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10760
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.027e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

QD
type: SiteQuality
SIO_000300: 1.542e1

FS
type: SiteQuality
SIO_000300: 2.921e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-1

DP
type: SiteQuality
SIO_000300: 1.481976e6

GenotypeDepth
all individuals: 13264
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12922
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13312
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3103
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 190
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3400
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27011
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2301
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 496
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4586
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60728
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.292323597828896e-4
allele num: 15476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9664
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6210
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.61e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.87e0

DP
type: SiteQuality
SIO_000300: 1.353842e6

FS
type: SiteQuality
SIO_000300: 1.908e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-1

GenotypeDepth
all individuals: 15319
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5119
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 225
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 136
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24136
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4070
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14926
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3649
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4242
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 9.704968944099378e-5
allele num: 10304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60224
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7674
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15384
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.066e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.304809e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.61e0

MQ
type: SiteQuality
SIO_000300: 5.797e1

QD
type: SiteQuality
SIO_000300: 1.356e1

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16926
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5050
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2289
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 734
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2694
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4406
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20414
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.055966209081309e-4
allele num: 9470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59096
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15194
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.131e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e0

MQ
type: SiteQuality
SIO_000300: 5.588e1

DP
type: SiteQuality
SIO_000300: 1.229642e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.837e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.078e1

GenotypeDepth
all individuals: 2827
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17446
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4700
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2917
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18608
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2880
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5419
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7538
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.591957811470006e-5
allele num: 15170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10052
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58956
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.606e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

FS
type: SiteQuality
SIO_000300: 7.849e0

QD
type: SiteQuality
SIO_000300: 1.093e1

DP
type: SiteQuality
SIO_000300: 1.209349e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

GenotypeDepth
all individuals: 11160
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 225
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4715
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2884
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5399
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19295
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2871
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17579
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.69606512890095e-5
allele num: 58960
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15176
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.207087e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.607e0

QD
type: SiteQuality
SIO_000300: 1.402e1

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.49e-1

GenotypeDepth
all individuals: 78
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18339
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6058
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3295
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5141
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16670
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 799
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2507
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.701258931609391e-5
allele num: 58780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7486
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

QD
type: SiteQuality
SIO_000300: 1.221e1

DP
type: SiteQuality
SIO_000300: 1.173457e6

MQ
type: SiteQuality
SIO_000300: 5.895e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.52e-1

GenotypeDepth
all individuals: 323
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2292
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1000
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3788
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5709
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13712
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19330
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6891
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5962
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.153779883695886e-4
allele num: 9286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.385761302615625e-4
allele num: 57730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14978
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

QD
type: SiteQuality
SIO_000300: 1.266e1

DP
type: SiteQuality
SIO_000300: 1.127085e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.148e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-2

GenotypeQuality
all individuals: 7393
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2014
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19854
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6111
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12287
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2284
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.743010527783588e-5
allele num: 57372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7298
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5930
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.099996e6

VQSLOD
type: SiteQuality
SIO_000300: 2.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.972e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.26e0

MQ
type: SiteQuality
SIO_000300: 5.395e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

QD
type: SiteQuality
SIO_000300: 5.83e0

GenotypeDepth
all individuals: 412
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 136
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6433
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 6308
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7687
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4323
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19945
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5894
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.277787551458429e-5
allele num: 56842
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.085151e6

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.518e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.88e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

MQ
type: SiteQuality
SIO_000300: 5.922e1

FS
type: SiteQuality
SIO_000300: 7.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

GenotypeDepth
all individuals: 173
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 136
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5601
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2285
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 151
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 348
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8759
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6727
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1224
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2296
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6375
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19343
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54176
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.472704542297541e-4
allele num: 14398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9124
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.023226e6

VQSLOD
type: SiteQuality
SIO_000300: -4.783e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

MQ
type: SiteQuality
SIO_000300: 5.89e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.362e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.24e-1

QD
type: SiteQuality
SIO_000300: 9.32e0

GenotypeDepth
all individuals: 260
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3710
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9694
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9151
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20443
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4712
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.164686699277894e-4
allele num: 8586
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64514
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.059e0

FS
type: SiteQuality
SIO_000300: 7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.208535e6

QD
type: SiteQuality
SIO_000300: 1.622e1

GenotypeDepth
all individuals: 584
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3243
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9149
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 478
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4713
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3707
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9693
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545595054095827e-5
allele num: 64700
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10774
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.772e0

QD
type: SiteQuality
SIO_000300: 1.01e1

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 9.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.699e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-1

DP
type: SiteQuality
SIO_000300: 2.217353e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeDepth
all individuals: 1874
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20829
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3317
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3706
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4712
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9148
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9694
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64760
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.737015806843842e-4
allele num: 11514
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10922
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

DP
type: SiteQuality
SIO_000300: 2.220109e6

QD
type: SiteQuality
SIO_000300: 1.571e1

GenotypeDepth
all individuals: 807
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3351
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3471
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3706
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9145
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4710
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21107
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.735202492211838e-5
allele num: 10272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64866
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11276
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.202e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.319e1

DP
type: SiteQuality
SIO_000300: 2.224662e6

FS
type: SiteQuality
SIO_000300: 2.973e0

VQSLOD
type: SiteQuality
SIO_000300: -6.625e-1

MQ
type: SiteQuality
SIO_000300: 5.832e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.79e-1

GenotypeDepth
all individuals: 1154
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3708
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9712
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 221
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9145
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3312
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 381
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21199
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4710
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.081664098613251e-5
allele num: 64900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.226208e6

VQSLOD
type: SiteQuality
SIO_000300: 3.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.519e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.93e-1

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

GenotypeDepth
all individuals: 1153
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 807
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3708
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9144
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 180
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22260
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2543
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4714
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9759
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65412
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 7.768800497203231e-5
allele num: 12872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.243464e6

VQSLOD
type: SiteQuality
SIO_000300: -1.834e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.037e0

MQRankSum
type: SiteQuality
SIO_000300: 9.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

MQ
type: SiteQuality
SIO_000300: 5.864e1

QD
type: SiteQuality
SIO_000300: 1.385e1

GenotypeDepth
all individuals: 9615
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1315
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 259
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1997
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2342
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4715
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2479
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9766
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3709
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9143
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65442
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.602e1

DP
type: SiteQuality
SIO_000300: 2.244524e6

FS
type: SiteQuality
SIO_000300: 2.619e0

MQRankSum
type: SiteQuality
SIO_000300: 9.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.304e0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.41e0

GenotypeDepth
all individuals: 366
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1315
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6247
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9837
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4723
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9142
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.883259911894274e-5
allele num: 14528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65994
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.264721e6

VQSLOD
type: SiteQuality
SIO_000300: 7.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.52e-1

QD
type: SiteQuality
SIO_000300: 1.337e1

FS
type: SiteQuality
SIO_000300: 6.529e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

GenotypeDepth
all individuals: 1153
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 205
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 366
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9142
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 161
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23851
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513546238837597e-5
allele num: 66070
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14750
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.23e-1

QD
type: SiteQuality
SIO_000300: 1.209e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 2.267533e6

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.015e0

MQ
type: SiteQuality
SIO_000300: 5.886e1

GenotypeDepth
all individuals: 16111
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 430
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4719
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24297
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2340
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9861
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9142
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 101
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3735
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66244
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.554798112218144e-5
allele num: 15256
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.274766e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 9.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.69e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

VQSLOD
type: SiteQuality
SIO_000300: -1.001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.244e0

MQRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

GenotypeDepth
all individuals: 205
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16122
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1315
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2340
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4720
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 583
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9143
bin: 9.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3739
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24857
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.178235443681668e-4
allele num: 15732
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.88e0

DP
type: SiteQuality
SIO_000300: 2.282239e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.76e-1

QD
type: SiteQuality
SIO_000300: 1.339e1

GenotypeDepth
all individuals: 1151
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 583
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6249
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9898
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1571
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4720
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2340
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25136
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9138
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3736
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.246096189881324e-5
allele num: 16010
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

FS
type: SiteQuality
SIO_000300: 6.062e0

QD
type: SiteQuality
SIO_000300: 1.364e1

VQSLOD
type: SiteQuality
SIO_000300: 7.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.285826e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.329e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.01e-1

GenotypeDepth
all individuals: 3406
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2340
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9137
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 8.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25163
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4719
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9901
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3733
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503488092374308e-5
allele num: 66512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.58e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

FS
type: SiteQuality
SIO_000300: 3.285e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 2.286363e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.263e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.015e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.006e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

GenotypeDepth
all individuals: 134
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3406
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1996
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9910
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4721
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3734
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9136
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25240
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16136
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.851e0

MQRankSum
type: SiteQuality
SIO_000300: 5.42e-1

DP
type: SiteQuality
SIO_000300: 2.287192e6

QD
type: SiteQuality
SIO_000300: 1.388e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e0

GenotypeDepth
all individuals: 1149
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4723
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2340
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3732
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25191
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 361
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9907
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9134
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1569
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16222
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66520
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.589e1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

DP
type: SiteQuality
SIO_000300: 2.287392e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.18e-1

GenotypeDepth
all individuals: 9616
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16124
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 365
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3466
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2340
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9133
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9903
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 387
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4720
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3731
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1568
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.730103806228374e-4
allele num: 11560
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66504
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

VQSLOD
type: SiteQuality
SIO_000300: 5.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.286834e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.89e0

FS
type: SiteQuality
SIO_000300: 1.818e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.481e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

GenotypeDepth
all individuals: 16130
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 429
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1996
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3730
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9900
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9131
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4723
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25198
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.51222813825467e-5
allele num: 66486
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16258
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.242e0

DP
type: SiteQuality
SIO_000300: 2.286543e6

VQSLOD
type: SiteQuality
SIO_000300: 7.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.43e0

QD
type: SiteQuality
SIO_000300: 1.378e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

GenotypeDepth
all individuals: 259
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9616
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9887
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9129
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3720
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3463
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4713
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25081
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505479947007106e-5
allele num: 66424
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: 10316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16258
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 1.351e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.4e-2

FS
type: SiteQuality
SIO_000300: 2.529e0

DP
type: SiteQuality
SIO_000300: 2.284462e6

GenotypeDepth
all individuals: 205
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 363
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3405
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3719
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 9.25e1
variant carriers: 0

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