3-33425467-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425467
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425467
    reference: chr 3
allele count: 550
allele frequency: 4.541026106771908e-3
allele num: 121118
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*869-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*581-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.774-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*632-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.748-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1424T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.952-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.175-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*730-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.700-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.964-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.748-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.82-14T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*991-14T>C
  variant of: http://identifiers.org/hgnc/13598
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6678
  bin: 3.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 26396
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 43
genotype quality: GenotypeQuality
num of homozygotes: 9
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

3-33425474-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425474
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425474
    reference: chr 3
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.748-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*991-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.964-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*869-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.952-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.700-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*730-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.774-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.82-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.748-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.175-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*632-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*581-7G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1431G>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26542
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.952-7G>T
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

3-33425476-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425476
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425477
    reference: chr 3
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*869-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*632-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1435dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.748-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*581-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*730-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.952-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.748-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.82-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.774-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.175-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.700-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.964-3dupC
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*991-3dupC
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.952-3dupC
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP

3-33425477-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425477
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425477
    reference: chr 3
allele count: 3
allele frequency: 2.474145182839329e-5
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*991-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.964-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.748-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.700-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*632-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*581-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.175-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*869-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.748-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.82-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.774-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.952-4C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1434C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*730-4C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.952-4C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-33425479-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425479
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425479
    reference: chr 3
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.748-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*632-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*730-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1436A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.82-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.175-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.700-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.952-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.964-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.774-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*869-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*581-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.748-2A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*991-2A>G
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.952-2A>G
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/3-33425483-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425483
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425483
    reference: chr 3
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: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1440C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.702C>A
  hgvsp: ENSP00000440794.1:p.Ser234Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.750C>A
  hgvsp: ENSP00000426163.1:p.Ser250Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*732C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*634C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.750C>A
  hgvsp: ENSP00000441228.1:p.Ser250Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.84C>A
  hgvsp: ENSP00000445039.1:p.Ser28Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.954C>A
  hgvsp: ENSP00000417601.1:p.Ser318Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*993C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.776C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*583C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.966C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.177C>A
  hgvsp: ENSP00000389251.3:p.Ser59Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*871C>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser318Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

3-33425486-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425486
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425486
    reference: chr 3
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*586G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.779G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.957G>C
  hgvsp: ENST00000484457.1:c.957G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*637G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.87G>C
  hgvsp: ENST00000542085.1:c.87G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*996G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.705G>C
  hgvsp: ENST00000538181.1:c.705G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1443G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.753G>C
  hgvsp: ENST00000538892.1:c.753G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*874G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.969G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*735G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.753G>C
  hgvsp: ENST00000507198.1:c.753G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.180G>C
  hgvsp: ENST00000446237.3:c.180G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu319Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

3-33425507-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425507
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425507
    reference: chr 3
allele count: 4
allele frequency: 3.29614186594591e-5
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.978A>G
  hgvsp: ENST00000484457.1:c.978A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.201A>G
  hgvsp: ENST00000446237.3:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.774A>G
  hgvsp: ENST00000507198.1:c.774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1017A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.726A>G
  hgvsp: ENST00000538181.1:c.726A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.990A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.774A>G
  hgvsp: ENST00000538892.1:c.774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*658A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.800A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*607A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.108A>G
  hgvsp: ENST00000542085.1:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1464A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*895A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*756A>G
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr326Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/3-33425519-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425519
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425519
    reference: chr 3
allele count: 8
allele frequency: 6.592392379194409e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1476C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.812C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.786C>A
  hgvsp: ENST00000507198.1:c.786C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.213C>A
  hgvsp: ENST00000446237.3:c.213C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*907C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*768C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*670C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1029C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1002C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.738C>A
  hgvsp: ENST00000538181.1:c.738C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.990C>A
  hgvsp: ENST00000484457.1:c.990C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*619C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.786C>A
  hgvsp: ENST00000538892.1:c.786C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.120C>A
  hgvsp: ENST00000542085.1:c.120C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile330Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

3-33425531-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425531
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425531
    reference: chr 3
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.798C>T
  hgvsp: ENST00000538892.1:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.750C>T
  hgvsp: ENST00000538181.1:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1002C>T
  hgvsp: ENST00000484457.1:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.798C>T
  hgvsp: ENST00000507198.1:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*780C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.225C>T
  hgvsp: ENST00000446237.3:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.132C>T
  hgvsp: ENST00000542085.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*919C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1014C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1041C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*631C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*682C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1488C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.824C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser334Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

3-33425537-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425537
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425537
    reference: chr 3
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.804T>G
  hgvsp: ENSP00000426163.1:p.Ser268Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.756T>G
  hgvsp: ENSP00000440794.1:p.Ser252Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*786T>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.804T>G
  hgvsp: ENSP00000441228.1:p.Ser268Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*925T>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*688T>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.138T>G
  hgvsp: ENSP00000445039.1:p.Ser46Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1020T>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1008T>G
  hgvsp: ENSP00000417601.1:p.Ser336Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*637T>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.231T>G
  hgvsp: ENSP00000389251.3:p.Ser77Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1047T>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.830T>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1494T>G
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser336Arg
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

3-33425543-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425543
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425543
    reference: chr 3
allele count: 257
allele frequency: 2.117596651395801e-3
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*694T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*643T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.810T>C
  hgvsp: ENST00000507198.1:c.810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*931T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*792T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.237T>C
  hgvsp: ENST00000446237.3:c.237T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1026T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.762T>C
  hgvsp: ENST00000538181.1:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.144T>C
  hgvsp: ENST00000542085.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1053T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1014T>C
  hgvsp: ENST00000484457.1:c.1014T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.836T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.810T>C
  hgvsp: ENST00000538892.1:c.810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1500T>C
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6767
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 26342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys338Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

3-33425549-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425549
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425549
    reference: chr 3
allele count: 8
allele frequency: 6.591849178490796e-5
allele num: 121362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.150T>C
  hgvsp: ENST00000542085.1:c.150T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*798T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.816T>C
  hgvsp: ENST00000538892.1:c.816T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1059T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1506T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.768T>C
  hgvsp: ENST00000538181.1:c.768T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.243T>C
  hgvsp: ENST00000446237.3:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*937T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1020T>C
  hgvsp: ENST00000484457.1:c.1020T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.816T>C
  hgvsp: ENST00000507198.1:c.816T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1032T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*649T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.842T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*700T>C
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6816
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His340His
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

3-33425558-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425558
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425558
    reference: chr 3
allele count: 3
allele frequency: 2.472065658063878e-5
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.825G>T
  hgvsp: ENST00000507198.1:c.825G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*709G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.252G>T
  hgvsp: ENST00000446237.3:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.851G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.777G>T
  hgvsp: ENST00000538181.1:c.777G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.159G>T
  hgvsp: ENST00000542085.1:c.159G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1068G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*946G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1029G>T
  hgvsp: ENST00000484457.1:c.1029G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.825G>T
  hgvsp: ENST00000538892.1:c.825G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1041G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1515G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*807G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*658G>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6822
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu343Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/3-33425559-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425559
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425559
    reference: chr 3
allele count: 11
allele frequency: 9.064390131351253e-5
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.778C>A
  hgvsp: ENST00000538181.1:c.778C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*710C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*808C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.852C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.253C>A
  hgvsp: ENST00000446237.3:c.253C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*659C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1030C>A
  hgvsp: ENST00000484457.1:c.1030C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.826C>A
  hgvsp: ENST00000507198.1:c.826C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.826C>A
  hgvsp: ENST00000538892.1:c.826C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.160C>A
  hgvsp: ENST00000542085.1:c.160C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1042C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1069C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*947C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1516C>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg344Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

3-33425559-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425559
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425559
    reference: chr 3
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.160C>T
  hgvsp: ENSP00000445039.1:p.Arg54Trp
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*808C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.253C>T
  hgvsp: ENSP00000389251.3:p.Arg85Trp
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1030C>T
  hgvsp: ENSP00000417601.1:p.Arg344Trp
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1042C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.778C>T
  hgvsp: ENSP00000440794.1:p.Arg260Trp
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*659C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*710C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.826C>T
  hgvsp: ENSP00000441228.1:p.Arg276Trp
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.826C>T
  hgvsp: ENSP00000426163.1:p.Arg276Trp
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1516C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*947C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1069C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.852C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg344Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

3-33425560-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425560
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425560
    reference: chr 3
allele count: 4
allele frequency: 3.29614186594591e-5
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1517G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.779G>A
  hgvsp: ENSP00000440794.1:p.Arg260Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1031G>A
  hgvsp: ENSP00000417601.1:p.Arg344Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.827G>A
  hgvsp: ENSP00000441228.1:p.Arg276Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*809G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.853G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.827G>A
  hgvsp: ENSP00000426163.1:p.Arg276Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*948G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1070G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.254G>A
  hgvsp: ENSP00000389251.3:p.Arg85Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.161G>A
  hgvsp: ENSP00000445039.1:p.Arg54Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*660G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1043G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*711G>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg344Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ

3-33425589-ATCACTGAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425589
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425581
    reference: chr 3
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.191_198delTCACTGAT
  hgvsp: ENSP00000445039.1:p.Ile64SerfsTer84
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.857_864delTCACTGAT
  hgvsp: ENSP00000441228.1:p.Ile286SerfsTer84
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.857_864delTCACTGAT
  hgvsp: ENSP00000426163.1:p.Ile286SerfsTer84
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.809_816delTCACTGAT
  hgvsp: ENSP00000440794.1:p.Ile270SerfsTer84
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.883_890delTCACTGAT
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.284_291delTCACTGAT
  hgvsp: ENSP00000389251.3:p.Ile95SerfsTer?
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsp: ENSP00000417601.1:p.Ile354SerfsTer84
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 6819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile354SerfsTer84
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: ATCACTGAT
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

3-33425597-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425597
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425597
    reference: chr 3
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1107T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.291T>C
  hgvsp: ENST00000446237.3:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*748T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*697T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1068T>C
  hgvsp: ENST00000484457.1:c.1068T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.864T>C
  hgvsp: ENST00000507198.1:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.890T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.864T>C
  hgvsp: ENST00000538892.1:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.198T>C
  hgvsp: ENST00000542085.1:c.198T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*985T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1554T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.816T>C
  hgvsp: ENST00000538181.1:c.816T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*846T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1080T>C
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp356Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-33425598-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425598
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425598
    reference: chr 3
allele count: 2
allele frequency: 1.648288252649623e-5
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1108G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1069G>A
  hgvsp: ENSP00000417601.1:p.Val357Met
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.865G>A
  hgvsp: ENSP00000441228.1:p.Val289Met
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.865G>A
  hgvsp: ENSP00000426163.1:p.Val289Met
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1081G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*749G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.292G>A
  hgvsp: ENSP00000389251.3:p.Val98Met
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*698G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*847G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*986G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.817G>A
  hgvsp: ENSP00000440794.1:p.Val273Met
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1555G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.199G>A
  hgvsp: ENSP00000445039.1:p.Val67Met
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.891G>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val357Met
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

3-33425612-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425612
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425612
    reference: chr 3
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.306C>T
  hgvsp: ENST00000446237.3:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.879C>T
  hgvsp: ENST00000538892.1:c.879C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1000C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1569C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1095C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.879C>T
  hgvsp: ENST00000507198.1:c.879C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.905C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*712C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.213C>T
  hgvsp: ENST00000542085.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.831C>T
  hgvsp: ENST00000538181.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*763C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1122C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1083C>T
  hgvsp: ENST00000484457.1:c.1083C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*861C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His361His
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

3-33425620-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425620
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425620
    reference: chr 3
allele count: 118
allele frequency: 9.730835202533315e-4
allele num: 121264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*869A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.221A>G
  hgvsp: ENSP00000445039.1:p.Asn74Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1103A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.887A>G
  hgvsp: ENSP00000441228.1:p.Asn296Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*771A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1008A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.887A>G
  hgvsp: ENSP00000426163.1:p.Asn296Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*720A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.839A>G
  hgvsp: ENSP00000440794.1:p.Asn280Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1577A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1130A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.913A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.314A>G
  hgvsp: ENSP00000389251.3:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1091A>G
  hgvsp: ENSP00000417601.1:p.Asn364Ser
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24282
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Asn364Ser
num of homozygotes: 1
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

3-33425626-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425626
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425626
    reference: chr 3
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1014G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.893G>A
  hgvsp: ENSP00000426163.1:p.Arg298Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*875G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.845G>A
  hgvsp: ENSP00000440794.1:p.Arg282Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1583G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*726G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.919G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.893G>A
  hgvsp: ENSP00000441228.1:p.Arg298Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.227G>A
  hgvsp: ENSP00000445039.1:p.Arg76Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1097G>A
  hgvsp: ENSP00000417601.1:p.Arg366Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1109G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*777G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.320G>A
  hgvsp: ENSP00000389251.3:p.Arg107Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1136G>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg366Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

3-33425638-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425638
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425638
    reference: chr 3
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*789G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1121G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1026G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1595G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.905G>A
  hgvsp: ENSP00000441228.1:p.Arg302His
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.905G>A
  hgvsp: ENSP00000426163.1:p.Arg302His
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.332G>A
  hgvsp: ENSP00000389251.3:p.Arg111His
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.857G>A
  hgvsp: ENSP00000440794.1:p.Arg286His
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1148G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1109G>A
  hgvsp: ENSP00000417601.1:p.Arg370His
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.239G>A
  hgvsp: ENSP00000445039.1:p.Arg80His
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.931G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*738G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*887G>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg370His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

3-33425642-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425642
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425642
    reference: chr 3
allele count: 2
allele frequency: 1.651364026686043e-5
allele num: 121112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*793C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.909C>T
  hgvsp: ENST00000538892.1:c.909C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1152C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*742C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.243C>T
  hgvsp: ENST00000542085.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1030C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1599C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1113C>T
  hgvsp: ENST00000484457.1:c.1113C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.861C>T
  hgvsp: ENST00000538181.1:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.909C>T
  hgvsp: ENST00000507198.1:c.909C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.336C>T
  hgvsp: ENST00000446237.3:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*891C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1125C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.935C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu371Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

3-33425648-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425648
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425648
    reference: chr 3
allele count: 4
allele frequency: 3.303328103063837e-5
allele num: 121090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*897G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.915G>T
  hgvsp: ENST00000507198.1:c.915G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.915G>T
  hgvsp: ENST00000538892.1:c.915G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.342G>T
  hgvsp: ENST00000446237.3:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*799G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1605G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.867G>T
  hgvsp: ENST00000538181.1:c.867G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1036G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1131G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1119G>T
  hgvsp: ENST00000484457.1:c.1119G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*748G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.249G>T
  hgvsp: ENST00000542085.1:c.249G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1158G>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.941G>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26021
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu373Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

3-33425651-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425651
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425651
    reference: chr 3
allele count: 10
allele frequency: 8.262414277451872e-5
allele num: 121030
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1122C>T
  hgvsp: ENST00000484457.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1039C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*802C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*751C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*900C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.918C>T
  hgvsp: ENST00000507198.1:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.918C>T
  hgvsp: ENST00000538892.1:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.870C>T
  hgvsp: ENST00000538181.1:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.345C>T
  hgvsp: ENST00000446237.3:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1161C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.252C>T
  hgvsp: ENST00000542085.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1134C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.944C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1608C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr374Tyr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP

3-33425657-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425657
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425657
    reference: chr 3
allele count: 1
allele frequency: 8.265829062654984e-6
allele num: 120980
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1045C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*757C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.924C>T
  hgvsp: ENST00000538892.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1614C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.351C>T
  hgvsp: ENST00000446237.3:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1140C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.924C>T
  hgvsp: ENST00000507198.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1128C>T
  hgvsp: ENST00000484457.1:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*808C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.258C>T
  hgvsp: ENST00000542085.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*906C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.876C>T
  hgvsp: ENST00000538181.1:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1167C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.950C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys376Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/3-33425670-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425670
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425670
    reference: chr 3
allele count: 2
allele frequency: 1.657824933687002e-5
allele num: 120640
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1180C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.271C>A
  hgvsp: ENSP00000445039.1:p.Arg91Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1058C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*770C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1141C>A
  hgvsp: ENSP00000417601.1:p.Arg381Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.889C>A
  hgvsp: ENSP00000440794.1:p.Arg297Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.937C>A
  hgvsp: ENSP00000441228.1:p.Arg313Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*821C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.937C>A
  hgvsp: ENSP00000426163.1:p.Arg313Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*919C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.364C>A
  hgvsp: ENSP00000389251.3:p.Arg122Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1627C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.963C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1153C>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25646
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg381Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

3-33425671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425671
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425671
    reference: chr 3
allele count: 3
allele frequency: 2.486572508454347e-5
allele num: 120648
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1142G>A
  hgvsp: ENSP00000417601.1:p.Arg381His
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*822G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.938G>A
  hgvsp: ENSP00000441228.1:p.Arg313His
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*771G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.890G>A
  hgvsp: ENSP00000440794.1:p.Arg297His
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.964G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*920G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1628G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1059G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1154G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.938G>A
  hgvsp: ENSP00000426163.1:p.Arg313His
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.272G>A
  hgvsp: ENSP00000445039.1:p.Arg91His
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1181G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.365G>A
  hgvsp: ENSP00000389251.3:p.Arg122His
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg381His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

3-33425692-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425692
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425692
    reference: chr 3
allele count: 1
allele frequency: 8.423748231012871e-6
allele num: 118712
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.959G>A
  hgvsp: ENSP00000426163.1:p.Arg320Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.985G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*941G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.911G>A
  hgvsp: ENSP00000440794.1:p.Arg304Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.293G>A
  hgvsp: ENSP00000445039.1:p.Arg98Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1202G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*843G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.959G>A
  hgvsp: ENSP00000441228.1:p.Arg320Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1080G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.386G>A
  hgvsp: ENSP00000389251.3:p.Arg129Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1649G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1163G>A
  hgvsp: ENSP00000417601.1:p.Arg388Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*792G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1175G>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 23217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg388Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

3-33425697-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425697
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425697
    reference: chr 3
allele count: 3
allele frequency: 2.534169045969827e-5
allele num: 118382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.960+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.912+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1176+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.960+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.986+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1650+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.387+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.294+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1081+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*844+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*942+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*793+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1203+4G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1164+4G>C
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22890
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1164+4G>C
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

3-33425700-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425700
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425700
    reference: chr 3
allele count: 1
allele frequency: 8.475581848693913e-6
allele num: 117986
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.294+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.986+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.960+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*942+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.960+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1176+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1650+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1203+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1164+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1081+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.912+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*844+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*793+7A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.387+7A>G
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1164+7A>G
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

3-33425702-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425702
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425702
    reference: chr 3
allele count: 1
allele frequency: 8.506873553831496e-6
allele num: 117552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*844+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1650+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1203+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.986+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1176+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.960+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.294+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.912+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1081+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.387+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*793+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.960+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1164+9G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*942+9G>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22175
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

3-33425703-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425703
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425703
    reference: chr 3
allele count: 6
allele frequency: 5.121201775349949e-5
allele num: 117160
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.960+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.986+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.912+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1164+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.387+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*793+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1203+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1650+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1176+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*844+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1081+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.960+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*942+10G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.294+10G>C
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

3-33425709-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425709
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425709
    reference: chr 3
allele count: 2
allele frequency: 1.72143705565406e-5
allele num: 116182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1176+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1164+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*942+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1650+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.387+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*844+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1081+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.960+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.294+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.986+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*793+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.960+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.912+16G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1203+16G>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20619
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19124
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

3-33425715-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425715
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425715
    reference: chr 3
allele count: 3
allele frequency: 2.600644959950068e-5
allele num: 115356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1203+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.986+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.294+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.912+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1081+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.960+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*844+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*942+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.387+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1176+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1164+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*793+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.960+22C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1650+22C>G
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17229
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  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: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/3-33425716-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425716
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425716
    reference: chr 3
allele count: 1
allele frequency: 8.674983083782986e-6
allele num: 115274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*942+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*793+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1081+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1203+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1650+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1176+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.912+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1164+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*844+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.387+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.960+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.294+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.986+23A>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.960+23A>C
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

3-33425720-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425720
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425720
    reference: chr 3
allele count: 1
allele frequency: 8.712015611931977e-6
allele num: 114784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1650+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.960+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.294+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.912+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.986+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1176+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1203+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1081+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.387+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*942+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*793+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1164+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.960+27A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*844+27A>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

3-33425723-C-CCTTGGCCAATAAAACTGCTCTCAAGGGGGTAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425723
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425756
    reference: chr 3
allele count: 1
allele frequency: 8.756107384900968e-6
allele num: 114206
alternate allele: CCTTGGCCAATAAAACTGCTCTCAAGGGGGTAAA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

3-33425723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425723
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425723
    reference: chr 3
allele count: 1
allele frequency: 8.756107384900968e-6
allele num: 114206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1203+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*793+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.986+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.960+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*844+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.960+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*942+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.912+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.387+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1650+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1164+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.294+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1081+30C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1176+30C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

3-33425727-A-AAATCTCCCCTGAAGATTTTATTTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425727
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425751
    reference: chr 3
allele count: 1
allele frequency: 8.786265310067303e-6
allele num: 113814
alternate allele: AAATCTCCCCTGAAGATTTTATTTC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

3-33425730-T-TCTTTACACAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425730
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425740
    reference: chr 3
allele count: 1
allele frequency: 8.821609414421567e-6
allele num: 113358
alternate allele: TCTTTACACAA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14162
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

3-33425737-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425737
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425737
    reference: chr 3
allele count: 1
allele frequency: 8.954315084439191e-6
allele num: 111678
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1081+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.387+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1176+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.960+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1164+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*942+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*793+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1650+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1203+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.294+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.960+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.986+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.912+44G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*844+44G>C
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16643
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

3-33425738-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33425738
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33425738
    reference: chr 3
allele count: 10
allele frequency: 8.975210468685491e-5
allele num: 111418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.986+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.387+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.960+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1176+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*942+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1081+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1203+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.912+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.294+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1164+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.960+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1650+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*844+45C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*793+45C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16594
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

3-33426947-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33426947
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33426947
    reference: chr 3
allele count: 2
allele frequency: 1.648016612007449e-5
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*943-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.961-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*794-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1651-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.295-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1177-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.961-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1082-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1165-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.913-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*845-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.388-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.987-46A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1204-46A>G
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6955
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7360
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

3-33426948-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33426948
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33426948
    reference: chr 3
allele count: 6
allele frequency: 4.944131316127757e-5
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.295-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*845-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.913-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.961-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1082-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1177-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*794-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1165-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1651-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.987-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.961-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1204-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*943-45A>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.388-45A>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6955
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5503
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-33426951-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33426951
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33426951
    reference: chr 3
allele count: 2648
allele frequency: 2.181938035596572e-2
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*943-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.961-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1082-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.913-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1177-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.295-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.987-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*845-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1165-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1651-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.961-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*794-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.388-42T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1204-42T>C
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 6.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 7.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 9.75e1
  variant carriers: 1681
genotype depth: GenotypeDepth
  all individuals: 8822
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 7767
  bin: 3.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 8.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 7336
  bin: 4.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 4.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 5.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 47
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

3-33426962-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33426962
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33426962
    reference: chr 3
allele count: 4
allele frequency: 3.295544423938835e-5
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.913-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.388-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.295-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1177-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*943-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1204-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1082-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.961-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.961-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.987-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*794-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1651-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1165-31A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*845-31A>G
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

3-33426968-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33426968
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33426968
    reference: chr 3
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1651-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*845-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.388-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*943-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.961-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.913-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1165-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1082-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.295-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*794-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.987-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1177-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.961-25T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1204-25T>C
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

3-33426970-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33426970
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33426970
    reference: chr 3
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.961-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1082-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.961-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1204-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*794-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1165-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*943-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.987-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.388-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1177-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.295-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.913-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1651-23C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*845-23C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

3-33426972-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33426972
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33426972
    reference: chr 3
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.388-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1204-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*845-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1177-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.295-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.961-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1651-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*794-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1082-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1165-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.961-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*943-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.987-21C>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.913-21C>G
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

3-33426973-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33426973
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33426973
    reference: chr 3
allele count: 7
allele frequency: 5.766062602965403e-5
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*943-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1204-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1651-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.987-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1177-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.388-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1082-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1165-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*845-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.961-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.961-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*794-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.913-20T>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.295-20T>C
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-33426979-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33426979
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33426979
    reference: chr 3
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1165-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.961-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.961-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1651-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.388-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.987-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*794-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1177-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1082-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.913-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.295-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*943-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1204-14C>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*845-14C>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

3-33427002-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33427002
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33427002
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1213C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*803C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1660C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1091C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.970C>T
  hgvsp: ENSP00000426163.1:p.Pro324Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.922C>T
  hgvsp: ENSP00000440794.1:p.Pro308Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.996C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1174C>T
  hgvsp: ENSP00000417601.1:p.Pro392Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1186C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*952C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.970C>T
  hgvsp: ENSP00000441228.1:p.Pro324Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.397C>T
  hgvsp: ENSP00000389251.3:p.Pro133Ser
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*854C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.304C>T
  hgvsp: ENSP00000445039.1:p.Pro102Ser
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7525
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro392Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

3-33427006-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33427006
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33427006
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1178A>G
  hgvsp: ENSP00000417601.1:p.His393Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1217A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.401A>G
  hgvsp: ENSP00000389251.3:p.His134Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.1000A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*858A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.926A>G
  hgvsp: ENSP00000440794.1:p.His309Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.974A>G
  hgvsp: ENSP00000426163.1:p.His325Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.308A>G
  hgvsp: ENSP00000445039.1:p.His103Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1095A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*956A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1190A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.974A>G
  hgvsp: ENSP00000441228.1:p.His325Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*807A>G
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1664A>G
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7161
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His393Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

3-33427010-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33427010
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33427010
    reference: chr 3
allele count: 5
allele frequency: 4.118276912939626e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1099C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*862C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*811C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1221C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1182C>T
  hgvsp: ENST00000484457.1:c.1182C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.930C>T
  hgvsp: ENST00000538181.1:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1194C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.405C>T
  hgvsp: ENST00000446237.3:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.1004C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.978C>T
  hgvsp: ENST00000538892.1:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.312C>T
  hgvsp: ENST00000542085.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*960C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.978C>T
  hgvsp: ENST00000507198.1:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1668C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val394Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

3-33427019-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33427019
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33427019
    reference: chr 3
allele count: 6
allele frequency: 4.942013705851344e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1203C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.987C>T
  hgvsp: ENST00000507198.1:c.987C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*820C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.321C>T
  hgvsp: ENST00000542085.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1191C>T
  hgvsp: ENST00000484457.1:c.1191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1108C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.939C>T
  hgvsp: ENST00000538181.1:c.939C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*969C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.414C>T
  hgvsp: ENST00000446237.3:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.1013C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1230C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.987C>T
  hgvsp: ENST00000538892.1:c.987C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*871C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1677C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His397His
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

3-33427034-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33427034
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33427034
    reference: chr 3
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1245C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*984C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.336C>T
  hgvsp: ENST00000542085.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*886C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1206C>T
  hgvsp: ENST00000484457.1:c.1206C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1218C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.1002C>T
  hgvsp: ENST00000507198.1:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.954C>T
  hgvsp: ENST00000538181.1:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.429C>T
  hgvsp: ENST00000446237.3:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1692C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.1002C>T
  hgvsp: ENST00000538892.1:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*835C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1123C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.1028C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9223
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro402Pro
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

3-33427035-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33427035
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33427035
    reference: chr 3
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*985G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.1029G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.1003G>A
  hgvsp: ENSP00000441228.1:p.Val335Ile
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.1003G>A
  hgvsp: ENSP00000426163.1:p.Val335Ile
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1246G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.955G>A
  hgvsp: ENSP00000440794.1:p.Val319Ile
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1207G>A
  hgvsp: ENSP00000417601.1:p.Val403Ile
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.430G>A
  hgvsp: ENSP00000389251.3:p.Val144Ile
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*836G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*887G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.337G>A
  hgvsp: ENSP00000445039.1:p.Val113Ile
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1124G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1693G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1219G>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val403Ile
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

3-33427045-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33427045
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33427045
    reference: chr 3
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*846C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*995C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.1013C>T
  hgvsp: ENSP00000426163.1:p.Pro338Leu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.965C>T
  hgvsp: ENSP00000440794.1:p.Pro322Leu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.1013C>T
  hgvsp: ENSP00000441228.1:p.Pro338Leu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1256C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.347C>T
  hgvsp: ENSP00000445039.1:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.440C>T
  hgvsp: ENSP00000389251.3:p.Pro147Leu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*897C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.1039C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1217C>T
  hgvsp: ENSP00000417601.1:p.Pro406Leu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1229C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1134C>T
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1703C>T
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro406Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

3-33427059-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33427059
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33427059
    reference: chr 3
allele count: 3
allele frequency: 2.471943441934048e-5
allele num: 121362
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1231G>C
  hgvsp: ENSP00000417601.1:p.Gly411Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.1027G>C
  hgvsp: ENSP00000426163.1:p.Gly343Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*911G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.1027G>C
  hgvsp: ENSP00000441228.1:p.Gly343Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*1009G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1270G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.1053G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.454G>C
  hgvsp: ENSP00000389251.3:p.Gly152Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.361G>C
  hgvsp: ENSP00000445039.1:p.Gly121Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1243G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1717G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.979G>C
  hgvsp: ENSP00000440794.1:p.Gly327Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1148G>C
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*860G>C
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly411Arg
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-33427060-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33427060
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33427060
    reference: chr 3
allele count: 10
allele frequency: 8.239811473113494e-5
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.455G>A
  hgvsp: ENSP00000389251.3:p.Gly152Glu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.980G>A
  hgvsp: ENSP00000440794.1:p.Gly327Glu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1232G>A
  hgvsp: ENSP00000417601.1:p.Gly411Glu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1149G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.362G>A
  hgvsp: ENSP00000445039.1:p.Gly121Glu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*861G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.1028G>A
  hgvsp: ENSP00000441228.1:p.Gly343Glu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1271G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*1010G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1718G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.1028G>A
  hgvsp: ENSP00000426163.1:p.Gly343Glu
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.1054G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1244G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*912G>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly411Glu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

3-33427064-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33427064
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33427064
    reference: chr 3
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.984T>A
  hgvsp: ENSP00000440794.1:p.Ser328Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.1032T>A
  hgvsp: ENSP00000426163.1:p.Ser344Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1153T>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*865T>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1248T>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.1058T>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.366T>A
  hgvsp: ENSP00000445039.1:p.Ser122Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*1014T>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.459T>A
  hgvsp: ENSP00000389251.3:p.Ser153Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1275T>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*916T>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.1032T>A
  hgvsp: ENSP00000441228.1:p.Ser344Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1236T>A
  hgvsp: ENSP00000417601.1:p.Ser412Arg
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1722T>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser412Arg
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

3-33427072-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33427072
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 33427072
    reference: chr 3
allele count: 2
allele frequency: 1.648206751054852e-5
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411273
  ensembl transcript: ENST00000432809
  gene symbol: FBXL2
  hgvsc: ENST00000432809.1:c.*924G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000463736
  gene symbol: FBXL2
  hgvsc: ENST00000463736.1:n.1066G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000406737
  ensembl transcript: ENST00000422741
  gene symbol: FBXL2
  hgvsc: ENST00000422741.1:c.*1022G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000440794
  ensembl transcript: ENST00000538181
  gene symbol: FBXL2
  hgvsc: ENST00000538181.1:c.992G>A
  hgvsp: ENSP00000440794.1:p.Arg331Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000441228
  ensembl transcript: ENST00000538892
  gene symbol: FBXL2
  hgvsc: ENST00000538892.1:c.1040G>A
  hgvsp: ENSP00000441228.1:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000445039
  ensembl transcript: ENST00000542085
  gene symbol: FBXL2
  hgvsc: ENST00000542085.1:c.374G>A
  hgvsp: ENSP00000445039.1:p.Arg125Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000464990
  gene symbol: FBXL2
  hgvsc: ENST00000464990.1:n.1730G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000416332
  ensembl transcript: ENST00000451636
  gene symbol: FBXL2
  hgvsc: ENST00000451636.1:c.*1161G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000426163
  ensembl transcript: ENST00000507198
  gene symbol: FBXL2
  hgvsc: ENST00000507198.1:c.1040G>A
  hgvsp: ENSP00000426163.1:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153558
  ensembl transcript: ENST00000283627
  gene symbol: FBXL2
  hgvsc: ENST00000283627.6:n.1256G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000389251
  ensembl transcript: ENST00000446237
  gene symbol: FBXL2
  hgvsc: ENST00000446237.3:c.467G>A
  hgvsp: ENSP00000389251.3:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000417601
  ensembl transcript: ENST00000484457
  gene symbol: FBXL2
  hgvsc: ENST00000484457.1:c.1244G>A
  hgvsp: ENSP00000417601.1:p.Arg415Gln
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000408895
  ensembl transcript: ENST00000421391
  gene symbol: FBXL2
  hgvsc: ENST00000421391.1:c.*873G>A
  variant of: http://identifiers.org/hgnc/13598
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000153558
  ensembl protein: ENSP00000411484
  ensembl transcript: ENST00000435207
  gene symbol: FBXL2
  hgvsc: ENST00000435207.1:c.*1283G>A
  variant of: http://identifiers.org/hgnc/13598
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4300
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg415Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

GenotypeDepth
all individuals: 362
bin: 4.75e1
variant carriers: 54

GenotypeDepth
all individuals: 87
bin: 1.75e1
variant carriers: 3

GenotypeDepth
all individuals: 67
bin: 6.25e1
variant carriers: 39

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 27

GenotypeDepth
all individuals: 42
bin: 7.25e1
variant carriers: 33

GenotypeDepth
all individuals: 23566
bin: 2.75e1
variant carriers: 21

GenotypeDepth
all individuals: 21
bin: 8.75e1
variant carriers: 14

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

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2144
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1408
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 159
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2320
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7613
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 9.75e1
variant carriers: 538

GenotypeQuality
all individuals: 552
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43430
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00336376741951e-5
allele num: 66592
num of homozygotes: 0

African
type: Population
allele count: 523
allele frequency: 5.037565016374494e-2
allele num: 10382
num of homozygotes: 9

Latino
type: Population
allele count: 24
allele frequency: 2.081165452653486e-3
allele num: 11532
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

DP
type: SiteQuality
SIO_000300: 1.589325e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.34e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.2e0

QD
type: SiteQuality
SIO_000300: 1.568e1

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 11
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 311
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2169
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7731
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 684
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1491
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 44024
bin: 6.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.121e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.58e-1

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.500045000450004e-5
allele num: 66666
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East Asian
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African
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Latino
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Other
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South Asian
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VQSLOD
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DP
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QD
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MQ
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16510
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African
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East Asian
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European (Finnish)
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

Other
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InbreedingCoeff
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BaseQRankSum
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MQ
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MQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

European (Non-Finnish)
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Other
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Latino
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African
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South Asian
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European (Finnish)
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VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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Latino
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MQRankSum
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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QD
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FS
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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South Asian
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FS
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InbreedingCoeff
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QD
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

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

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

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

Other
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 4.239341085271318e-4
allele num: 16512
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -8.44e-1

MQ
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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QD
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BaseQRankSum
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SIO_000300: -4.107e0

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.02e-1

MQRankSum
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SIO_000300: 2.85e-1

ClippingRankSum
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SIO_000300: 2.1e-1

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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DP
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SIO_000300: 1.579422e6

BaseQRankSum
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SIO_000300: -1.683e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.74e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 7.72e-1

BaseQRankSum
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SIO_000300: 3.98e0

MQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

DP
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SIO_000300: 1.579513e6

ClippingRankSum
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SIO_000300: -2.83e-1

FS
type: SiteQuality
SIO_000300: 4.286e0

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

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 28
allele frequency: 1.695736434108527e-3
allele num: 16512
num of homozygotes: 0

East Asian
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allele count: 0
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African
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allele count: 5
allele frequency: 4.808617041738796e-4
allele num: 10398
num of homozygotes: 0

European (Finnish)
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allele count: 6
allele frequency: 9.071666162685213e-4
allele num: 6614
num of homozygotes: 0

Other
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allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 205
allele frequency: 3.072726182624858e-3
allele num: 66716
num of homozygotes: 0

Latino
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allele count: 11
allele frequency: 9.504060825989287e-4
allele num: 11574
num of homozygotes: 0

VQSLOD
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SIO_000300: 3.85e0

BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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DP
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MQ
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SIO_000300: 5.975e1

ClippingRankSum
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SIO_000300: 1.21e-1

ReadPosRankSum
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SIO_000300: 2.84e-1

QD
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SIO_000300: 1.266e1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 8
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allele num: 66716
num of homozygotes: 0

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

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

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

East Asian
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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Latino
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allele frequency: 0.0e0
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African
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.496807266840543e-5
allele num: 66714
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 2

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

European (Finnish)
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South Asian
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African
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allele num: 10398
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Latino
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European (Non-Finnish)
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Other
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MQRankSum
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QD
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InbreedingCoeff
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DP
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FS
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 66714
num of homozygotes: 0

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

South Asian
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East Asian
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Latino
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European (Non-Finnish)
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African
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Other
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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DP
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FS
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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South Asian
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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ClippingRankSum
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DP
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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DP
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QD
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InbreedingCoeff
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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: 906
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: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

QD
type: SiteQuality
SIO_000300: 1.176e1

FS
type: SiteQuality
SIO_000300: 4.916e0

MQRankSum
type: SiteQuality
SIO_000300: 9.47e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 1.578839e6

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

GenotypeDepth
all individuals: 9
bin: 9.25e1
variant carriers: 4

GenotypeDepth
all individuals: 26159
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 6.25e1
variant carriers: 8

GenotypeDepth
all individuals: 14
bin: 8.75e1
variant carriers: 8

GenotypeDepth
all individuals: 1839
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 19
bin: 7.75e1
variant carriers: 8

GenotypeDepth
all individuals: 58
bin: 5.75e1
variant carriers: 8

GenotypeQuality
all individuals: 534
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7726
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2317
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 121
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1381
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 9.75e1
variant carriers: 117

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 116
allele frequency: 1.117964533538936e-2
allele num: 10376
num of homozygotes: 1

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
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: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 1.336e1

VQSLOD
type: SiteQuality
SIO_000300: 6.37e0

DP
type: SiteQuality
SIO_000300: 1.583966e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

GenotypeDepth
all individuals: 26148
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 24331
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variant carriers: 0

GenotypeDepth
all individuals: 74
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variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
all individuals: 11
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variant carriers: 0

GenotypeDepth
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7735
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44169
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1387
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.828e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

MQRankSum
type: SiteQuality
SIO_000300: 2.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.677e0

QD
type: SiteQuality
SIO_000300: 1.045e1

VQSLOD
type: SiteQuality
SIO_000300: -1.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.577171e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.76e-1

GenotypeDepth
all individuals: 121
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26065
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
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variant carriers: 1

GenotypeDepth
all individuals: 15
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variant carriers: 0

GenotypeDepth
all individuals: 51
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variant carriers: 0

GenotypeDepth
all individuals: 727
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 2315
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 44031
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1388
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 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: 11556
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501726986033939e-5
allele num: 66590
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-1

DP
type: SiteQuality
SIO_000300: 1.575632e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

FS
type: SiteQuality
SIO_000300: 2.825e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-2

QD
type: SiteQuality
SIO_000300: 9.449999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.395e0

GenotypeDepth
all individuals: 24296
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1843
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
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variant carriers: 0

GenotypeDepth
all individuals: 51
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variant carriers: 0

GenotypeDepth
all individuals: 27
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variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2149
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 7685
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variant carriers: 0

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 236
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 530
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

GenotypeQuality
all individuals: 43978
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
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GenotypeQuality
all individuals: 1385
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

FS
type: SiteQuality
SIO_000300: 9.007e0

MQRankSum
type: SiteQuality
SIO_000300: -4.13e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.575074e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.27e-1

GenotypeDepth
all individuals: 28
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 114
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 201
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variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 10
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variant carriers: 0

GenotypeDepth
all individuals: 9
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variant carriers: 0

GenotypeDepth
all individuals: 52
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variant carriers: 0

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

GenotypeQuality
all individuals: 529
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variant carriers: 0

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 1383
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variant carriers: 0

GenotypeQuality
all individuals: 266
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variant carriers: 0

GenotypeQuality
all individuals: 648
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 2308
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 44007
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 2145
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variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 7684
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.010518407212622e-5
allele num: 66550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 6.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

DP
type: SiteQuality
SIO_000300: 1.574396e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.317e0

QD
type: SiteQuality
SIO_000300: 1.267e1

FS
type: SiteQuality
SIO_000300: 6.985e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 24273
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variant carriers: 0

GenotypeDepth
all individuals: 305
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variant carriers: 1

GenotypeDepth
all individuals: 120
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variant carriers: 0

GenotypeDepth
all individuals: 5
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GenotypeDepth
all individuals: 13
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 12
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variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2301
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 301
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GenotypeQuality
all individuals: 43903
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 55
bin: 3.75e1
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GenotypeQuality
all individuals: 7675
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

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

GenotypeQuality
all individuals: 648
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variant carriers: 0

GenotypeQuality
all individuals: 527
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66518
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.060606060606061e-4
allele num: 16500
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
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SIO_000300: 1.244e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.21e-1

BaseQRankSum
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SIO_000300: 2.35e0

VQSLOD
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SIO_000300: 8.86e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.574043e6

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503714174009804e-5
allele num: 66502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.963e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

MQ
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SIO_000300: 5.971e1

DP
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SIO_000300: 1.572558e6

VQSLOD
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SIO_000300: 2.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.929e0

QD
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SIO_000300: 8.75e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.708737864077671e-5
allele num: 10300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508295625942685e-5
allele num: 66300
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e-1

FS
type: SiteQuality
SIO_000300: 7.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.568151e6

VQSLOD
type: SiteQuality
SIO_000300: -1.484e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.52420449404313e-5
allele num: 66310
num of homozygotes: 0

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.084e0

FS
type: SiteQuality
SIO_000300: 6.67e0

DP
type: SiteQuality
SIO_000300: 1.566974e6

ReadPosRankSum
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SIO_000300: -3.8e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: -8.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

QD
type: SiteQuality
SIO_000300: 1.187e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65258
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.11545988258317e-5
allele num: 16352
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -1.96e0

InbreedingCoeff
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DP
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SIO_000300: 1.51948e6

VQSLOD
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MQ
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QD
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ClippingRankSum
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SIO_000300: 1.91e0

MQRankSum
type: SiteQuality
SIO_000300: 4.94e-1

FS
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 3
allele frequency: 2.986857825567503e-4
allele num: 10044
num of homozygotes: 0

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

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

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

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

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

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

Latino
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allele frequency: 8.901548869503294e-5
allele num: 11234
num of homozygotes: 0

European (Non-Finnish)
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allele num: 64836
num of homozygotes: 0

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

South Asian
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ClippingRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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BaseQRankSum
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DP
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FS
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MQRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 1.584283903675539e-4
allele num: 6312
num of homozygotes: 0

African
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South Asian
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East Asian
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Latino
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BaseQRankSum
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DP
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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allele frequency: 0.0e0
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African
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European (Finnish)
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allele frequency: 9.56327701625757e-4
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Other
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East Asian
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European (Non-Finnish)
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MQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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QD
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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Other
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African
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Latino
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South Asian
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East Asian
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BaseQRankSum
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MQRankSum
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MQ
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FS
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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Other
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East Asian
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South Asian
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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FS
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DP
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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African
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East Asian
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VQSLOD
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FS
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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African
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Latino
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East Asian
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European (Finnish)
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ClippingRankSum
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MQ
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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VQSLOD
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FS
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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African
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ReadPosRankSum
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FS
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MQ
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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South Asian
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Other
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European (Finnish)
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MQRankSum
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FS
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DP
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VQSLOD
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QD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Other
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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FS
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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East Asian
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African
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European (Finnish)
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South Asian
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DP
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

QD
type: SiteQuality
SIO_000300: 1.528e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: -4.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.32e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.28e0

DP
type: SiteQuality
SIO_000300: 2.870165e6

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-1

GenotypeDepth
all individuals: 721
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4249
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 909
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variant carriers: 0

GenotypeDepth
all individuals: 1899
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variant carriers: 0

GenotypeDepth
all individuals: 2223
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variant carriers: 3

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4288
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25109
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3876
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.994693131052679e-5
allele num: 66706
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

FS
type: SiteQuality
SIO_000300: 9.84e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

DP
type: SiteQuality
SIO_000300: 2.870338e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -8.159999999999999e-1

GenotypeDepth
all individuals: 422
bin: 9.25e1
variant carriers: 104

GenotypeDepth
all individuals: 19
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variant carriers: 2

GenotypeDepth
all individuals: 131
bin: 1.75e1
variant carriers: 8

GenotypeDepth
all individuals: 1684
bin: 2.25e1
variant carriers: 7

GenotypeDepth
all individuals: 74
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variant carriers: 0

GenotypeDepth
all individuals: 4205
bin: 5.75e1
variant carriers: 75

GenotypeDepth
all individuals: 2925
bin: 6.25e1
variant carriers: 69

GenotypeQuality
all individuals: 11507
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variant carriers: 0

GenotypeQuality
all individuals: 6313
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
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variant carriers: 0

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

GenotypeQuality
all individuals: 4497
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variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3864
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4275
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variant carriers: 1

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2779
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25210
bin: 9.75e1
variant carriers: 2600

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 37
allele frequency: 3.559746007311911e-3
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 153
allele frequency: 1.321928460342146e-2
allele num: 11574
num of homozygotes: 2

South Asian
type: Population
allele count: 789
allele frequency: 4.778921865536039e-2
allele num: 16510
num of homozygotes: 24

European (Non-Finnish)
type: Population
allele count: 1600
allele frequency: 2.398441013341328e-2
allele num: 66710
num of homozygotes: 20

European (Finnish)
type: Population
allele count: 46
allele frequency: 6.954944058058663e-3
allele num: 6614
num of homozygotes: 1

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

Other
type: Population
allele count: 23
allele frequency: 2.533039647577092e-2
allele num: 908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.96e0

QD
type: SiteQuality
SIO_000300: 1.627e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e0

DP
type: SiteQuality
SIO_000300: 2.923196e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.37e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

GenotypeDepth
all individuals: 1274
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1854
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variant carriers: 0

GenotypeDepth
all individuals: 831
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variant carriers: 0

GenotypeDepth
all individuals: 1027
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variant carriers: 4

GenotypeDepth
all individuals: 334
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variant carriers: 0

GenotypeDepth
all individuals: 9215
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GenotypeDepth
all individuals: 462
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4686
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 4446
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 23566
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variant carriers: 4

GenotypeQuality
all individuals: 2913
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 6597
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 12328
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variant carriers: 0

GenotypeQuality
all individuals: 2056
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 4005
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 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: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.624277456647399e-4
allele num: 8650
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.53e0

QD
type: SiteQuality
SIO_000300: 1.409e1

DP
type: SiteQuality
SIO_000300: 2.742754e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

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

GenotypeDepth
all individuals: 9215
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 334
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variant carriers: 0

GenotypeDepth
all individuals: 608
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variant carriers: 0

GenotypeDepth
all individuals: 1853
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variant carriers: 0

GenotypeDepth
all individuals: 7600
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variant carriers: 0

GenotypeDepth
all individuals: 1274
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variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4696
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

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

GenotypeQuality
all individuals: 2059
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variant carriers: 0

GenotypeQuality
all individuals: 6600
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 4006
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 2913
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 12368
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GenotypeQuality
all individuals: 23564
bin: 9.75e1
variant carriers: 1

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

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

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: 10400
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 9.473000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.291e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

DP
type: SiteQuality
SIO_000300: 2.742831e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.32e-1

QD
type: SiteQuality
SIO_000300: 1.438e1

VQSLOD
type: SiteQuality
SIO_000300: -1.929e-1

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

GenotypeDepth
all individuals: 1023
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1273
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2984
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 462
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variant carriers: 0

GenotypeDepth
all individuals: 334
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variant carriers: 0

GenotypeDepth
all individuals: 7601
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

GenotypeQuality
all individuals: 12380
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GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2059
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

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

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 4692
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23564
bin: 9.75e1
variant carriers: 2

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: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.13e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.064e1

VQSLOD
type: SiteQuality
SIO_000300: 6.31e-1

FS
type: SiteQuality
SIO_000300: 1.789e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.151e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.743002e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.19e-1

GenotypeDepth
all individuals: 2984
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1853
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7598
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1273
bin: 7.25e1
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GenotypeDepth
all individuals: 1023
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 5600
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variant carriers: 0

GenotypeDepth
all individuals: 1877
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 2059
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

GenotypeQuality
all individuals: 4446
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GenotypeQuality
all individuals: 23563
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variant carriers: 4

GenotypeQuality
all individuals: 4690
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GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 12386
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variant carriers: 0

GenotypeQuality
all individuals: 4006
bin: 9.25e1
variant carriers: 0

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

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

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: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.993946114424431e-5
allele num: 66734
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.74309e6

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.77e-1

QD
type: SiteQuality
SIO_000300: 2.358e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeDepth
all individuals: 1853
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7161
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 333
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variant carriers: 0

GenotypeDepth
all individuals: 830
bin: 7.75e1
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

African
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European (Non-Finnish)
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South Asian
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East Asian
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allele frequency: 8.090614886731392e-4
allele num: 8652
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10406
num of homozygotes: 0

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

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

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

Latino
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African
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European (Finnish)
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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South Asian
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African
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Latino
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Other
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European (Finnish)
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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ClippingRankSum
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DP
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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Latino
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 2.311604253351826e-4
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African
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European (Non-Finnish)
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Other
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num of homozygotes: 0

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

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

Other
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Latino
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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QD
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 10

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.923816852635629e-4
allele num: 10396
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

QD
type: SiteQuality
SIO_000300: 1.313e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e0