7-100189245-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189245
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189245
    reference: chr 7
allele count: 1
allele frequency: 8.495310588555118e-6
allele num: 117712
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.338-45G>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.281-45G>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.364-45G>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.561-45G>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.437-45G>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.40-45G>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1203C>G
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.281-45G>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.323-45G>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.287-45G>C
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7793
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19603
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

7-100189250-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189250
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189250
    reference: chr 7
allele count: 1
allele frequency: 8.460380040271409e-6
allele num: 118198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.40-40A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.364-40A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1198T>C
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.281-40A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.561-40A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.287-40A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.437-40A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.338-40A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.323-40A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.281-40A>G
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15104
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7872
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

7-100189255-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189255
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189255
    reference: chr 7
allele count: 14
allele frequency: 1.181394720853305e-4
allele num: 118504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.287-35A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.338-35A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.40-35A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.281-35A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.561-35A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1193T>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.437-35A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.323-35A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.281-35A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.364-35A>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22859
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15734
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8558
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3453
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

7-100189261-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189261
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189261
    reference: chr 7
allele count: 1
allele frequency: 8.408024618696084e-6
allele num: 118934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.323-29T>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.364-29T>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.287-29T>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.281-29T>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.281-29T>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.561-29T>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.40-29T>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.338-29T>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.437-29T>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1187A>C
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16378
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1516
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5144
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-100189262-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189262
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189262
    reference: chr 7
allele count: 1
allele frequency: 8.404208827780952e-6
allele num: 118988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.364-28G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.561-28G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.338-28G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.323-28G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.40-28G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.281-28G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.287-28G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1186C>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.281-28G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.437-28G>A
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

7-100189262-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189262
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189261
    reference: chr 7
allele count: 1
allele frequency: 8.404208827780952e-6
allele num: 118988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.287-26delA
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.281-26delA
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1185delT
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.437-26delA
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.561-26delA
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.40-26delA
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.281-26delA
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.364-26delA
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.323-26delA
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.338-26delA
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: GA
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/7-100189265-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189265
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189265
    reference: chr 7
allele count: 5
allele frequency: 4.192379930238798e-5
allele num: 119264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.364-25C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1183G>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.281-25C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.338-25C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.561-25C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.281-25C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.437-25C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.323-25C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.40-25C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.287-25C>A
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3646
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8999
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

7-100189265-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189265
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189265
    reference: chr 7
allele count: 39
allele frequency: 3.270056345586262e-4
allele num: 119264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.561-25C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.40-25C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.437-25C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.338-25C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.281-25C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.287-25C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.323-25C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.364-25C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.281-25C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1183G>C
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8999
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3646
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23958
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16763
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

7-100189265-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189265
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189265
    reference: chr 7
allele count: 4
allele frequency: 3.353903944191038e-5
allele num: 119264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.364-25C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1183G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.281-25C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.40-25C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.437-25C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.561-25C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.323-25C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.281-25C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.287-25C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.338-25C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16763
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3646
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

7-100189272-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189272
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189272
    reference: chr 7
allele count: 1
allele frequency: 8.345294922722569e-6
allele num: 119828
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.287-18T>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.323-18T>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.338-18T>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.281-18T>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.281-18T>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1176A>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.437-18T>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.40-18T>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.561-18T>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.364-18T>A
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3222
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

7-100189276-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189276
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189276
    reference: chr 7
allele count: 1
allele frequency: 8.320713584396998e-6
allele num: 120182
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.437-14C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1172G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.40-14C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.287-14C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.281-14C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.281-14C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.338-14C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.364-14C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.561-14C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.323-14C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5152
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/7-100189291-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189291
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189291
    reference: chr 7
allele count: 1
allele frequency: 8.274720728175424e-6
allele num: 120850
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.324C>A
  hgvsp: ENSP00000241071.6:p.Tyr108Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.339C>A
  hgvsp: ENSP00000417179.1:p.Tyr113Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.282C>A
  hgvsp: ENSP00000419602.1:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1157G>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.365C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.438C>A
  hgvsp: ENSP00000416558.2:p.Tyr146Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.288C>A
  hgvsp: ENSP00000420239.1:p.Tyr96Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.282C>A
  hgvsp: ENSP00000353821.2:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.41C>A
  hgvsp: ENSP00000418814.1:p.Thr14Lys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.562C>A
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr146Ter
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

7-100189291-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189291
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189291
    reference: chr 7
allele count: 1
allele frequency: 8.274720728175424e-6
allele num: 120850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.41C>T
  hgvsp: ENSP00000418814.1:p.Thr14Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.282C>T
  hgvsp: ENST00000465843.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.282C>T
  hgvsp: ENST00000360609.2:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.438C>T
  hgvsp: ENST00000427939.2:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.339C>T
  hgvsp: ENST00000466053.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.288C>T
  hgvsp: ENST00000468962.1:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.562C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1157G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.365C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.324C>T
  hgvsp: ENST00000241071.6:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr14Ile
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

7-100189293-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189293
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189293
    reference: chr 7
allele count: 2
allele frequency: 1.654478673769895e-5
allele num: 120884
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.341C>T
  hgvsp: ENSP00000417179.1:p.Thr114Met
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.564C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.43C>T
  hgvsp: ENSP00000418814.1:p.Arg15Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.326C>T
  hgvsp: ENSP00000241071.6:p.Thr109Met
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.284C>T
  hgvsp: ENSP00000419602.1:p.Thr95Met
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.440C>T
  hgvsp: ENSP00000416558.2:p.Thr147Met
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.367C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1155G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.284C>T
  hgvsp: ENSP00000353821.2:p.Thr95Met
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.290C>T
  hgvsp: ENSP00000420239.1:p.Thr97Met
  variant of: http://identifiers.org/hgnc/13595
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4516
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg15Ter
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

7-100189294-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189294
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189294
    reference: chr 7
allele count: 40
allele frequency: 3.307862789851477e-4
allele num: 120924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.285G>A
  hgvsp: ENST00000465843.1:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.441G>A
  hgvsp: ENST00000427939.2:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.368G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.327G>A
  hgvsp: ENST00000241071.6:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.342G>A
  hgvsp: ENST00000466053.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.285G>A
  hgvsp: ENST00000360609.2:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.44G>A
  hgvsp: ENSP00000418814.1:p.Arg15Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.291G>A
  hgvsp: ENST00000468962.1:c.291G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.565G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1154C>T
  variant of: http://identifiers.org/hgnc/40430
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17935
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24820
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3658
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg15Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP

7-100189297-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189297
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189297
    reference: chr 7
allele count: 1
allele frequency: 8.265282507356101e-6
allele num: 120988
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.444G>A
  hgvsp: ENST00000427939.2:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.47G>A
  hgvsp: ENSP00000418814.1:p.Arg16Lys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.345G>A
  hgvsp: ENST00000466053.1:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.371G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.568G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.288G>A
  hgvsp: ENST00000360609.2:c.288G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.294G>A
  hgvsp: ENST00000468962.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.288G>A
  hgvsp: ENST00000465843.1:c.288G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1151C>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.330G>A
  hgvsp: ENST00000241071.6:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg16Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

7-100189301-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189301
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189301
    reference: chr 7
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.292C>T
  hgvsp: ENST00000465843.1:c.292C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.448C>T
  hgvsp: ENST00000427939.2:c.448C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1147G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.292C>T
  hgvsp: ENST00000360609.2:c.292C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.334C>T
  hgvsp: ENST00000241071.6:c.334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.349C>T
  hgvsp: ENST00000466053.1:c.349C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.298C>T
  hgvsp: ENST00000468962.1:c.298C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.51C>T
  hgvsp: ENST00000488079.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.375C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.572C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5164
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu150Leu
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

7-100189318-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189318
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189318
    reference: chr 7
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.392T>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.465T>C
  hgvsp: ENST00000427939.2:c.465T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1130A>G
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.309T>C
  hgvsp: ENST00000360609.2:c.309T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.351T>C
  hgvsp: ENST00000241071.6:c.351T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.315T>C
  hgvsp: ENST00000468962.1:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.68T>C
  hgvsp: ENSP00000418814.1:p.Leu23Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.309T>C
  hgvsp: ENST00000465843.1:c.309T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.366T>C
  hgvsp: ENST00000466053.1:c.366T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.589T>C
  variant of: http://identifiers.org/hgnc/13595
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu23Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

7-100189325-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189325
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189325
    reference: chr 7
allele count: 50
allele frequency: 4.124051468162323e-4
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.322C>T
  hgvsp: ENSP00000420239.1:p.Arg108Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.316C>T
  hgvsp: ENSP00000419602.1:p.Arg106Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.316C>T
  hgvsp: ENSP00000353821.2:p.Arg106Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.358C>T
  hgvsp: ENSP00000241071.6:p.Arg120Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.373C>T
  hgvsp: ENSP00000417179.1:p.Arg125Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.75C>T
  hgvsp: ENST00000488079.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1123G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.472C>T
  hgvsp: ENSP00000416558.2:p.Arg158Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.596C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.399C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9421
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24665
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1837
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg158Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

7-100189326-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189326
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189326
    reference: chr 7
allele count: 3
allele frequency: 2.474145182839329e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.374G>A
  hgvsp: ENSP00000417179.1:p.Arg125His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.317G>A
  hgvsp: ENSP00000419602.1:p.Arg106His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.317G>A
  hgvsp: ENSP00000353821.2:p.Arg106His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.76G>A
  hgvsp: ENSP00000418814.1:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.597G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.400G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1122C>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.359G>A
  hgvsp: ENSP00000241071.6:p.Arg120His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.473G>A
  hgvsp: ENSP00000416558.2:p.Arg158His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.323G>A
  hgvsp: ENSP00000420239.1:p.Arg108His
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg158His
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

7-100189327-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189327
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189327
    reference: chr 7
allele count: 2
allele frequency: 1.649103712132456e-5
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.474C>G
  hgvsp: ENST00000427939.2:c.474C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.318C>G
  hgvsp: ENST00000360609.2:c.318C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.77C>G
  hgvsp: ENSP00000418814.1:p.Ala26Gly
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.324C>G
  hgvsp: ENST00000468962.1:c.324C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.598C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.375C>G
  hgvsp: ENST00000466053.1:c.375C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.318C>G
  hgvsp: ENST00000465843.1:c.318C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.360C>G
  hgvsp: ENST00000241071.6:c.360C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1121G>C
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.401C>G
  variant of: http://identifiers.org/hgnc/13595
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18425
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala26Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

7-100189328-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189328
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189328
    reference: chr 7
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.475C>T
  hgvsp: ENSP00000416558.2:p.Arg159Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.402C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.319C>T
  hgvsp: ENSP00000353821.2:p.Arg107Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.599C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.361C>T
  hgvsp: ENSP00000241071.6:p.Arg121Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.325C>T
  hgvsp: ENSP00000420239.1:p.Arg109Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1120G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.319C>T
  hgvsp: ENSP00000419602.1:p.Arg107Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.376C>T
  hgvsp: ENSP00000417179.1:p.Arg126Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.78C>T
  hgvsp: ENST00000488079.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg159Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

7-100189329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189329
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189329
    reference: chr 7
allele count: 2
allele frequency: 1.648994937585542e-5
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.320G>A
  hgvsp: ENSP00000419602.1:p.Arg107His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.403G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.326G>A
  hgvsp: ENSP00000420239.1:p.Arg109His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1119C>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.377G>A
  hgvsp: ENSP00000417179.1:p.Arg126His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.476G>A
  hgvsp: ENSP00000416558.2:p.Arg159His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.600G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.79G>A
  hgvsp: ENSP00000418814.1:p.Ala27Thr
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.362G>A
  hgvsp: ENSP00000241071.6:p.Arg121His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.320G>A
  hgvsp: ENSP00000353821.2:p.Arg107His
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg159His
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

7-100189331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189331
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189331
    reference: chr 7
allele count: 2
allele frequency: 1.648695881557688e-5
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.322C>T
  hgvsp: ENSP00000353821.2:p.Arg108Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.602C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.328C>T
  hgvsp: ENSP00000420239.1:p.Arg110Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.364C>T
  hgvsp: ENSP00000241071.6:p.Arg122Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.81C>T
  hgvsp: ENST00000488079.1:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.322C>T
  hgvsp: ENSP00000419602.1:p.Arg108Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.379C>T
  hgvsp: ENSP00000417179.1:p.Arg127Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1117G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.478C>T
  hgvsp: ENSP00000416558.2:p.Arg160Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.405C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3674
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg160Ter
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

7-100189332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189332
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189332
    reference: chr 7
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.323G>A
  hgvsp: ENSP00000419602.1:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.365G>A
  hgvsp: ENSP00000241071.6:p.Arg122Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.479G>A
  hgvsp: ENSP00000416558.2:p.Arg160Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.603G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.406G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.380G>A
  hgvsp: ENSP00000417179.1:p.Arg127Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.82G>A
  hgvsp: ENSP00000418814.1:p.Asp28Asn
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.323G>A
  hgvsp: ENSP00000353821.2:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.329G>A
  hgvsp: ENSP00000420239.1:p.Arg110Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1116C>T
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8822
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1844
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg160Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

7-100189333-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189333
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189333
    reference: chr 7
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.604A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.324A>G
  hgvsp: ENST00000465843.1:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.324A>G
  hgvsp: ENST00000360609.2:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.480A>G
  hgvsp: ENST00000427939.2:c.480A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.381A>G
  hgvsp: ENST00000466053.1:c.381A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.330A>G
  hgvsp: ENST00000468962.1:c.330A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.366A>G
  hgvsp: ENST00000241071.6:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.83A>G
  hgvsp: ENSP00000418814.1:p.Asp28Gly
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1115T>C
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.407A>G
  variant of: http://identifiers.org/hgnc/13595
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31784
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp28Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

7-100189346-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189346
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189346
    reference: chr 7
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.337A>T
  hgvsp: ENSP00000353821.2:p.Ser113Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.337A>T
  hgvsp: ENSP00000419602.1:p.Ser113Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.379A>T
  hgvsp: ENSP00000241071.6:p.Ser127Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.343A>T
  hgvsp: ENSP00000420239.1:p.Ser115Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.96A>T
  hgvsp: ENSP00000418814.1:p.Arg32Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.617A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1102T>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.493A>T
  hgvsp: ENSP00000416558.2:p.Ser165Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.420A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.394A>T
  hgvsp: ENSP00000417179.1:p.Ser132Cys
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5174
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser165Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

7-100189348-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189348
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189348
    reference: chr 7
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.345C>T
  hgvsp: ENST00000468962.1:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.619C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.339C>T
  hgvsp: ENST00000360609.2:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.381C>T
  hgvsp: ENST00000241071.6:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.422C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.98C>T
  hgvsp: ENSP00000418814.1:p.Ala33Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.495C>T
  hgvsp: ENST00000427939.2:c.495C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.339C>T
  hgvsp: ENST00000465843.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.396C>T
  hgvsp: ENST00000466053.1:c.396C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1100G>A
  variant of: http://identifiers.org/hgnc/40430
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3676
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala33Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

7-100189350-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189350
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189350
    reference: chr 7
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.398T>C
  hgvsp: ENSP00000417179.1:p.Val133Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.621T>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.341T>C
  hgvsp: ENSP00000353821.2:p.Val114Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.347T>C
  hgvsp: ENSP00000420239.1:p.Val116Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.341T>C
  hgvsp: ENSP00000419602.1:p.Val114Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.497T>C
  hgvsp: ENSP00000416558.2:p.Val166Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1098A>G
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.424T>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.383T>C
  hgvsp: ENSP00000241071.6:p.Val128Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.100T>C
  hgvsp: ENSP00000418814.1:p.Trp34Arg
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9470
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val166Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

7-100189352-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189352
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189352
    reference: chr 7
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.343G>T
  hgvsp: ENSP00000419602.1:p.Ala115Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.400G>T
  hgvsp: ENSP00000417179.1:p.Ala134Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.343G>T
  hgvsp: ENSP00000353821.2:p.Ala115Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.349G>T
  hgvsp: ENSP00000420239.1:p.Ala117Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.102G>T
  hgvsp: ENSP00000418814.1:p.Trp34Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.385G>T
  hgvsp: ENSP00000241071.6:p.Ala129Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.499G>T
  hgvsp: ENSP00000416558.2:p.Ala167Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.426G>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.623G>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1096C>A
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3677
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala167Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

7-100189353-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189353
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189353
    reference: chr 7
allele count: 3
allele frequency: 2.471536142096851e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.350C>T
  hgvsp: ENSP00000420239.1:p.Ala117Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1095G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.401C>T
  hgvsp: ENSP00000417179.1:p.Ala134Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.103C>T
  hgvsp: ENSP00000418814.1:p.Pro35Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.344C>T
  hgvsp: ENSP00000419602.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.344C>T
  hgvsp: ENSP00000353821.2:p.Ala115Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.500C>T
  hgvsp: ENSP00000416558.2:p.Ala167Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.624C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.386C>T
  hgvsp: ENSP00000241071.6:p.Ala129Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.427C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala167Val
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: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

7-100189369-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189369
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189369
    reference: chr 7
allele count: 4
allele frequency: 3.305020325875004e-5
allele num: 121028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.402C>T
  hgvsp: ENST00000241071.6:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.360C>T
  hgvsp: ENST00000360609.2:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.417C>T
  hgvsp: ENST00000466053.1:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.516C>T
  hgvsp: ENST00000427939.2:c.516C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.366C>T
  hgvsp: ENST00000468962.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.640C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1079G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.360C>T
  hgvsp: ENST00000465843.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.443C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*5C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His172His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

7-100189373-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189373
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189373
    reference: chr 7
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.364T>C
  hgvsp: ENSP00000353821.2:p.Tyr122His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.406T>C
  hgvsp: ENSP00000241071.6:p.Tyr136His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.520T>C
  hgvsp: ENSP00000416558.2:p.Tyr174His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.370T>C
  hgvsp: ENSP00000420239.1:p.Tyr124His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.421T>C
  hgvsp: ENSP00000417179.1:p.Tyr141His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.364T>C
  hgvsp: ENSP00000419602.1:p.Tyr122His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.644T>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*9T>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1075A>G
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.447T>C
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr174His
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/7-100189375-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189375
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189375
    reference: chr 7
allele count: 35
allele frequency: 2.89768681800871e-4
allele num: 120786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.366C>A
  hgvsp: ENSP00000419602.1:p.Tyr122Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*11C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1073G>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.522C>A
  hgvsp: ENSP00000416558.2:p.Tyr174Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.449C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.646C>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.372C>A
  hgvsp: ENSP00000420239.1:p.Tyr124Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.423C>A
  hgvsp: ENSP00000417179.1:p.Tyr141Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.408C>A
  hgvsp: ENSP00000241071.6:p.Tyr136Ter
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.366C>A
  hgvsp: ENSP00000353821.2:p.Tyr122Ter
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24168
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18268
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9527
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1451
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr174Ter
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

7-100189376-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189376
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189376
    reference: chr 7
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.367C>T
  hgvsp: ENSP00000353821.2:p.Arg123Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1072G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.424C>T
  hgvsp: ENSP00000417179.1:p.Arg142Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.647C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.523C>T
  hgvsp: ENSP00000416558.2:p.Arg175Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*12C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.367C>T
  hgvsp: ENSP00000419602.1:p.Arg123Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.409C>T
  hgvsp: ENSP00000241071.6:p.Arg137Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.450C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.373C>T
  hgvsp: ENSP00000420239.1:p.Arg125Cys
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg175Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

7-100189379-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189379
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189379
    reference: chr 7
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.412C>T
  hgvsp: ENSP00000241071.6:p.Arg138Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.370C>T
  hgvsp: ENSP00000419602.1:p.Arg124Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1069G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.526C>T
  hgvsp: ENSP00000416558.2:p.Arg176Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.650C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*15C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.376C>T
  hgvsp: ENSP00000420239.1:p.Arg126Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.427C>T
  hgvsp: ENSP00000417179.1:p.Arg143Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.370C>T
  hgvsp: ENSP00000353821.2:p.Arg124Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.453C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg176Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

7-100189381-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189381
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189381
    reference: chr 7
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.652C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.528C>T
  hgvsp: ENST00000427939.2:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.372C>T
  hgvsp: ENST00000360609.2:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.429C>T
  hgvsp: ENST00000466053.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.414C>T
  hgvsp: ENST00000241071.6:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.455C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.378C>T
  hgvsp: ENST00000468962.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.372C>T
  hgvsp: ENST00000465843.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1067G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3657
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg176Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS

7-100189388-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189388
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189388
    reference: chr 7
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*24C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.436C>T
  hgvsp: ENSP00000417179.1:p.Pro146Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.385C>T
  hgvsp: ENSP00000420239.1:p.Pro129Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.535C>T
  hgvsp: ENSP00000416558.2:p.Pro179Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.421C>T
  hgvsp: ENSP00000241071.6:p.Pro141Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1060G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.379C>T
  hgvsp: ENSP00000353821.2:p.Pro127Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.462C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.659C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.379C>T
  hgvsp: ENSP00000419602.1:p.Pro127Ser
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8809
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro179Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-100189389-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189389
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189389
    reference: chr 7
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.536C>T
  hgvsp: ENSP00000416558.2:p.Pro179Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.380C>T
  hgvsp: ENSP00000419602.1:p.Pro127Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*25C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.437C>T
  hgvsp: ENSP00000417179.1:p.Pro146Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.422C>T
  hgvsp: ENSP00000241071.6:p.Pro141Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.380C>T
  hgvsp: ENSP00000353821.2:p.Pro127Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.386C>T
  hgvsp: ENSP00000420239.1:p.Pro129Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.660C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.463C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1059G>A
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9607
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5257
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro179Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

7-100189390-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189390
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189390
    reference: chr 7
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*26C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.423C>G
  hgvsp: ENST00000241071.6:c.423C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.387C>G
  hgvsp: ENST00000468962.1:c.387C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.537C>G
  hgvsp: ENST00000427939.2:c.537C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.381C>G
  hgvsp: ENST00000465843.1:c.381C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.661C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.438C>G
  hgvsp: ENST00000466053.1:c.438C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.381C>G
  hgvsp: ENST00000360609.2:c.381C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.464C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1058G>C
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro179Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

7-100189392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189392
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189392
    reference: chr 7
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.383C>T
  hgvsp: ENSP00000419602.1:p.Thr128Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.383C>T
  hgvsp: ENSP00000353821.2:p.Thr128Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.389C>T
  hgvsp: ENSP00000420239.1:p.Thr130Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.425C>T
  hgvsp: ENSP00000241071.6:p.Thr142Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*28C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.440C>T
  hgvsp: ENSP00000417179.1:p.Thr147Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.539C>T
  hgvsp: ENSP00000416558.2:p.Thr180Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1056G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.663C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.466C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr180Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

7-100189396-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189396
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189396
    reference: chr 7
allele count: 8
allele frequency: 6.589677270555675e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.470G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*32G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.393G>A
  hgvsp: ENST00000468962.1:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1052C>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.543G>A
  hgvsp: ENST00000427939.2:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.387G>A
  hgvsp: ENST00000465843.1:c.387G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.429G>A
  hgvsp: ENST00000241071.6:c.429G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.444G>A
  hgvsp: ENST00000466053.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.667G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.387G>A
  hgvsp: ENST00000360609.2:c.387G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys181Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-100189398-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189398
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189398
    reference: chr 7
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*34A>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.389A>C
  hgvsp: ENSP00000419602.1:p.Asp130Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.395A>C
  hgvsp: ENSP00000420239.1:p.Asp132Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.472A>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.389A>C
  hgvsp: ENSP00000353821.2:p.Asp130Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.446A>C
  hgvsp: ENSP00000417179.1:p.Asp149Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.545A>C
  hgvsp: ENSP00000416558.2:p.Asp182Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1050T>G
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.669A>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.431A>C
  hgvsp: ENSP00000241071.6:p.Asp144Ala
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3657
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp182Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

7-100189398-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189398
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189398
    reference: chr 7
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.389A>G
  hgvsp: ENSP00000353821.2:p.Asp130Gly
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.472A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.545A>G
  hgvsp: ENSP00000416558.2:p.Asp182Gly
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1050T>C
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.446A>G
  hgvsp: ENSP00000417179.1:p.Asp149Gly
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*34A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.395A>G
  hgvsp: ENSP00000420239.1:p.Asp132Gly
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.431A>G
  hgvsp: ENSP00000241071.6:p.Asp144Gly
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.389A>G
  hgvsp: ENSP00000419602.1:p.Asp130Gly
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.669A>G
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  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: 9603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3255
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp182Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD

7-100189402-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189402
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189402
    reference: chr 7
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.393C>T
  hgvsp: ENST00000360609.2:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.393C>T
  hgvsp: ENST00000465843.1:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.435C>T
  hgvsp: ENST00000241071.6:c.435C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.399C>T
  hgvsp: ENST00000468962.1:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1046G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.549C>T
  hgvsp: ENST00000427939.2:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.673C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.476C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.450C>T
  hgvsp: ENST00000466053.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His183His
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

7-100189403-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189403
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189403
    reference: chr 7
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.400G>A
  hgvsp: ENSP00000420239.1:p.Val134Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*39G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.394G>A
  hgvsp: ENSP00000353821.2:p.Val132Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.436G>A
  hgvsp: ENSP00000241071.6:p.Val146Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.674G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.550G>A
  hgvsp: ENSP00000416558.2:p.Val184Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.451G>A
  hgvsp: ENSP00000417179.1:p.Val151Ile
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.477G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1045C>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.394G>A
  hgvsp: ENSP00000419602.1:p.Val132Ile
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3255
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5260
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val184Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

7-100189408-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189408
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189408
    reference: chr 7
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1040G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*44C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.456C>T
  hgvsp: ENST00000466053.1:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.482C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.441C>T
  hgvsp: ENST00000241071.6:c.441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.555C>T
  hgvsp: ENST00000427939.2:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.399C>T
  hgvsp: ENST00000360609.2:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.399C>T
  hgvsp: ENST00000465843.1:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.405C>T
  hgvsp: ENST00000468962.1:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.679C>T
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe185Phe
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

7-100189420-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189420
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189420
    reference: chr 7
allele count: 65
allele frequency: 5.35393637876217e-4
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.417C>T
  hgvsp: ENST00000468962.1:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.567C>T
  hgvsp: ENST00000427939.2:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.411C>T
  hgvsp: ENST00000465843.1:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.494C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.453C>T
  hgvsp: ENST00000241071.6:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1028G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.691C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.468C>T
  hgvsp: ENST00000466053.1:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*56C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.411C>T
  hgvsp: ENST00000360609.2:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr189Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

7-100189421-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189421
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189421
    reference: chr 7
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1027C>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.568G>A
  hgvsp: ENSP00000416558.2:p.Val190Met
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.692G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.454G>A
  hgvsp: ENSP00000241071.6:p.Val152Met
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.469G>A
  hgvsp: ENSP00000417179.1:p.Val157Met
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.495G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.412G>A
  hgvsp: ENSP00000419602.1:p.Val138Met
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.418G>A
  hgvsp: ENSP00000420239.1:p.Val140Met
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.412G>A
  hgvsp: ENSP00000353821.2:p.Val138Met
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*57G>A
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val190Met
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

7-100189424-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189424
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189424
    reference: chr 7
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.472G>A
  hgvsp: ENSP00000417179.1:p.Gly158Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.498G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1024C>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.571G>A
  hgvsp: ENSP00000416558.2:p.Gly191Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.415G>A
  hgvsp: ENSP00000419602.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.457G>A
  hgvsp: ENSP00000241071.6:p.Gly153Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.415G>A
  hgvsp: ENSP00000353821.2:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*60G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.421G>A
  hgvsp: ENSP00000420239.1:p.Gly141Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.695G>A
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly191Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

7-100189438-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189438
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189438
    reference: chr 7
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.709C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*74C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1010G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.429C>T
  hgvsp: ENST00000465843.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.471C>T
  hgvsp: ENST00000241071.6:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.486C>T
  hgvsp: ENST00000466053.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.435C>T
  hgvsp: ENST00000468962.1:c.435C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.585C>T
  hgvsp: ENST00000427939.2:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.512C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.429C>T
  hgvsp: ENST00000360609.2:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe195Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

7-100189443-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189443
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189443
    reference: chr 7
allele count: 3
allele frequency: 2.471128976458378e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.517A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.434A>G
  hgvsp: ENSP00000419602.1:p.Lys145Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*79A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.714A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.491A>G
  hgvsp: ENSP00000417179.1:p.Lys164Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.590A>G
  hgvsp: ENSP00000416558.2:p.Lys197Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.434A>G
  hgvsp: ENSP00000353821.2:p.Lys145Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.476A>G
  hgvsp: ENSP00000241071.6:p.Lys159Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.440A>G
  hgvsp: ENSP00000420239.1:p.Lys147Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+1005T>C
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys197Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

7-100189451-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189451
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189451
    reference: chr 7
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*87C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.598C>G
  hgvsp: ENSP00000416558.2:p.Leu200Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.442C>G
  hgvsp: ENSP00000419602.1:p.Leu148Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.525C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.442C>G
  hgvsp: ENSP00000353821.2:p.Leu148Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.484C>G
  hgvsp: ENSP00000241071.6:p.Leu162Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.448C>G
  hgvsp: ENSP00000420239.1:p.Leu150Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.499C>G
  hgvsp: ENSP00000417179.1:p.Leu167Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.722C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+997G>C
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu200Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

7-100189453-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189453
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189453
    reference: chr 7
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*89G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.724G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.527G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.600G>A
  hgvsp: ENST00000427939.2:c.600G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+995C>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.450G>A
  hgvsp: ENST00000468962.1:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.444G>A
  hgvsp: ENST00000360609.2:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.486G>A
  hgvsp: ENST00000241071.6:c.486G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.444G>A
  hgvsp: ENST00000465843.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.501G>A
  hgvsp: ENST00000466053.1:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu200Leu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

7-100189462-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189462
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189462
    reference: chr 7
allele count: 25
allele frequency: 2.059308072487644e-4
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.453C>T
  hgvsp: ENST00000360609.2:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.609C>T
  hgvsp: ENST00000427939.2:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.495C>T
  hgvsp: ENST00000241071.6:c.495C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.536C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*98C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.733C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.459C>T
  hgvsp: ENST00000468962.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.510C>T
  hgvsp: ENST00000466053.1:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+986G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.453C>T
  hgvsp: ENST00000465843.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 24175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr203Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

7-100189465-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189465
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189465
    reference: chr 7
allele count: 10
allele frequency: 8.237639422047218e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.539C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+983G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.456C>T
  hgvsp: ENST00000465843.1:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.736C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.462C>T
  hgvsp: ENST00000468962.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*101C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.498C>T
  hgvsp: ENST00000241071.6:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.513C>T
  hgvsp: ENST00000466053.1:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.612C>T
  hgvsp: ENST00000427939.2:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.456C>T
  hgvsp: ENST00000360609.2:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5274
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu204Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP

7-100189466-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189466
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189466
    reference: chr 7
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*102G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.499G>A
  hgvsp: ENSP00000241071.6:p.Gly167Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000498195
  gene symbol: FBXO24
  hgvsc: ENST00000498195.1:n.540G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.514G>A
  hgvsp: ENSP00000417179.1:p.Gly172Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.457G>A
  hgvsp: ENSP00000419602.1:p.Gly153Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.613G>A
  hgvsp: ENSP00000416558.2:p.Gly205Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+982C>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.457G>A
  hgvsp: ENSP00000353821.2:p.Gly153Ser
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.737G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.463G>A
  hgvsp: ENSP00000420239.1:p.Gly155Ser
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1852
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly205Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

7-100189472-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189472
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189472
    reference: chr 7
allele count: 104
allele frequency: 8.567709620549322e-4
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.743A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.469A>G
  hgvsp: ENSP00000420239.1:p.Met157Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.619A>G
  hgvsp: ENSP00000416558.2:p.Met207Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.463A>G
  hgvsp: ENSP00000419602.1:p.Met155Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.463A>G
  hgvsp: ENSP00000353821.2:p.Met155Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.505A>G
  hgvsp: ENSP00000241071.6:p.Met169Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*108A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.520A>G
  hgvsp: ENSP00000417179.1:p.Met174Val
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+976T>C
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met207Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

7-100189476-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189476
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189476
    reference: chr 7
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*112A>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+972T>C
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.473A>G
  hgvsp: ENSP00000420239.1:p.Gln158Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.524A>G
  hgvsp: ENSP00000417179.1:p.Gln175Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.467A>G
  hgvsp: ENSP00000419602.1:p.Gln156Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.623A>G
  hgvsp: ENSP00000416558.2:p.Gln208Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.467A>G
  hgvsp: ENSP00000353821.2:p.Gln156Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.509A>G
  hgvsp: ENSP00000241071.6:p.Gln170Arg
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.747A>G
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln208Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

7-100189476-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189476
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189476
    reference: chr 7
allele count: 3
allele frequency: 2.471536142096851e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.473A>T
  hgvsp: ENSP00000420239.1:p.Gln158Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.524A>T
  hgvsp: ENSP00000417179.1:p.Gln175Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.467A>T
  hgvsp: ENSP00000353821.2:p.Gln156Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.747A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.623A>T
  hgvsp: ENSP00000416558.2:p.Gln208Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*112A>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.467A>T
  hgvsp: ENSP00000419602.1:p.Gln156Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.509A>T
  hgvsp: ENSP00000241071.6:p.Gln170Leu
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+972T>A
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8783
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln208Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

7-100189485-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189485
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189485
    reference: chr 7
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*121G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.476G>A
  hgvsp: ENSP00000419602.1:p.Arg159Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.476G>A
  hgvsp: ENSP00000353821.2:p.Arg159Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.533G>A
  hgvsp: ENSP00000417179.1:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.518G>A
  hgvsp: ENSP00000241071.6:p.Arg173Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.632G>A
  hgvsp: ENSP00000416558.2:p.Arg211Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.756G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.482G>A
  hgvsp: ENSP00000420239.1:p.Arg161Gln
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+963C>T
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg211Gln
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

7-100189493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189493
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189493
    reference: chr 7
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.484C>T
  hgvsp: ENSP00000419602.1:p.Arg162Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.526C>T
  hgvsp: ENSP00000241071.6:p.Arg176Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+955G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*129C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.640C>T
  hgvsp: ENSP00000416558.2:p.Arg214Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.490C>T
  hgvsp: ENSP00000420239.1:p.Arg164Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.541C>T
  hgvsp: ENSP00000417179.1:p.Arg181Cys
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.764C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.484C>T
  hgvsp: ENSP00000353821.2:p.Arg162Cys
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg214Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

7-100189494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189494
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189494
    reference: chr 7
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*130G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.765G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.485G>A
  hgvsp: ENSP00000353821.2:p.Arg162His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.485G>A
  hgvsp: ENSP00000419602.1:p.Arg162His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+954C>T
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.491G>A
  hgvsp: ENSP00000420239.1:p.Arg164His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.641G>A
  hgvsp: ENSP00000416558.2:p.Arg214His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.542G>A
  hgvsp: ENSP00000417179.1:p.Arg181His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.527G>A
  hgvsp: ENSP00000241071.6:p.Arg176His
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1851
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg214His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

7-100189495-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189495
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189495
    reference: chr 7
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.486C>T
  hgvsp: ENST00000465843.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.492C>T
  hgvsp: ENST00000468962.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.486C>T
  hgvsp: ENST00000360609.2:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.528C>T
  hgvsp: ENST00000241071.6:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.766C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.642C>T
  hgvsp: ENST00000427939.2:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+953G>A
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*131C>T
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.543C>T
  hgvsp: ENST00000466053.1:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg214Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

7-100189512-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189512
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189512
    reference: chr 7
allele count: 2
allele frequency: 1.649566164098842e-5
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.545G>A
  hgvsp: ENSP00000241071.6:p.Arg182His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.503G>A
  hgvsp: ENSP00000353821.2:p.Arg168His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.509G>A
  hgvsp: ENSP00000420239.1:p.Arg170His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.560G>A
  hgvsp: ENSP00000417179.1:p.Arg187His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*148G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.503G>A
  hgvsp: ENSP00000419602.1:p.Arg168His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.659G>A
  hgvsp: ENSP00000416558.2:p.Arg220His
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.783G>A
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+936C>T
  variant of: http://identifiers.org/hgnc/40430
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24089
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1851
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3640
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg220His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

7-100189515-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189515
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189515
    reference: chr 7
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.786G>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*151G>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.662G>C
  hgvsp: ENSP00000416558.2:p.Gly221Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.506G>C
  hgvsp: ENSP00000353821.2:p.Gly169Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000417179
  ensembl transcript: ENST00000466053
  gene symbol: FBXO24
  hgvsc: ENST00000466053.1:c.563G>C
  hgvsp: ENST00000466053.1:c.563G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.548G>C
  hgvsp: ENSP00000241071.6:p.Gly183Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.512G>C
  hgvsp: ENSP00000420239.1:p.Gly171Ala
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+933C>G
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.506G>C
  hgvsp: ENSP00000419602.1:p.Gly169Ala
  variant of: http://identifiers.org/hgnc/13595
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8705
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3248
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly221Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-100189540-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189540
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189540
    reference: chr 7
allele count: 1
allele frequency: 8.269793751343841e-6
allele num: 120922
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.558+15C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+908G>C
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.522+15C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*161+15C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.516+15C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.516+15C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.672+15C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.811C>G
  variant of: http://identifiers.org/hgnc/13595
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3619
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30588
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4480
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3242
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

7-100189549-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189549
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189549
    reference: chr 7
allele count: 3
allele frequency: 2.484019474712682e-5
allele num: 120772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.516+24T>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+899A>G
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.558+24T>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.672+24T>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*161+24T>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.516+24T>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.820T>C
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.522+24T>C
  variant of: http://identifiers.org/hgnc/13595
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8529
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29810
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-100189555-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100189555
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 100189555
    reference: chr 7
allele count: 4
allele frequency: 3.316419593406958e-5
allele num: 120612
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000420239
  ensembl transcript: ENST00000468962
  gene symbol: FBXO24
  hgvsc: ENST00000468962.1:c.522+30C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106336
  ensembl transcript: ENST00000474649
  gene symbol: FBXO24
  hgvsc: ENST00000474649.1:n.826C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000224729
  ensembl transcript: ENST00000442166
  gene symbol: PCOLCE-AS1
  hgvsc: ENST00000442166.2:n.1754+893G>C
  variant of: http://identifiers.org/hgnc/40430
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000416558
  ensembl transcript: ENST00000427939
  gene symbol: FBXO24
  hgvsc: ENST00000427939.2:c.672+30C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000418814
  ensembl transcript: ENST00000488079
  gene symbol: FBXO24
  hgvsc: ENST00000488079.1:c.*161+30C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000353821
  ensembl transcript: ENST00000360609
  gene symbol: FBXO24
  hgvsc: ENST00000360609.2:c.516+30C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000241071
  ensembl transcript: ENST00000241071
  gene symbol: FBXO24
  hgvsc: ENST00000241071.6:c.558+30C>G
  variant of: http://identifiers.org/hgnc/13595
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106336
  ensembl protein: ENSP00000419602
  ensembl transcript: ENST00000465843
  gene symbol: FBXO24
  hgvsc: ENST00000465843.1:c.516+30C>G
  variant of: http://identifiers.org/hgnc/13595
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22085
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8374
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3224
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 833
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28364
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3551
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 1219
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2955
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2951
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2764
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5112
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1337
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2196
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1692
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7416
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3201
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4100
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541544627716972e-5
allele num: 64870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16184
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9960
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

MQRankSum
type: SiteQuality
SIO_000300: -2.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.550301e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

QD
type: SiteQuality
SIO_000300: 1.381e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

FS
type: SiteQuality
SIO_000300: 3.276e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.14e0

GenotypeQuality
all individuals: 5129
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3039
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3333
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4271
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1830
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24155
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1935
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.536051119781266e-5
allele num: 65102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e0

QD
type: SiteQuality
SIO_000300: 1.384e1

VQSLOD
type: SiteQuality
SIO_000300: -1.629e0

FS
type: SiteQuality
SIO_000300: 3.332e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.257e0

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.566e0

MQ
type: SiteQuality
SIO_000300: 5.87e1

DP
type: SiteQuality
SIO_000300: 1.586392e6

GenotypeQuality
all individuals: 4355
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5146
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 26586
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8068
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 1.231310466138962e-3
allele num: 11370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65284
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.613164e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e0

QD
type: SiteQuality
SIO_000300: 1.427e1

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 236
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3546
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8269
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28205
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3183
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4406
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1816
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6314
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.762705923589205e-5
allele num: 11412
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

DP
type: SiteQuality
SIO_000300: 1.636887e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.3e-3

QD
type: SiteQuality
SIO_000300: 1.064e1

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.91e0

GenotypeQuality
all individuals: 842
bin: 3.25e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6310
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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10066
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.52597204419215e-5
allele num: 65532
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

VQSLOD
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ReadPosRankSum
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DP
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MQ
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SIO_000300: 5.905e1

FS
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SIO_000300: 0.0e0

QD
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InbreedingCoeff
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SIO_000300: 1.4e-3

BaseQRankSum
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SIO_000300: -2.18e0

MQRankSum
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SIO_000300: 1.58e0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10066
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.52597204419215e-5
allele num: 65532
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6310
num of homozygotes: 0

DP
type: SiteQuality
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QD
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MQRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 9.98e-1

VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.829714564527934e-4
allele num: 16396
num of homozygotes: 0

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

Other
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: 1
allele frequency: 1.180916391119509e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.522579859313621e-5
allele num: 65678
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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MQRankSum
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DP
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QD
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: 1.82e0

FS
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SIO_000300: 2.043e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.146788990825688e-3
allele num: 872
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 1.98373338623289e-4
allele num: 10082
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 frequency: 6.099048548426445e-5
allele num: 16396
num of homozygotes: 0

European (Non-Finnish)
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allele count: 33
allele frequency: 5.024513535734949e-4
allele num: 65678
num of homozygotes: 0

Latino
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allele frequency: 1.746724890829694e-4
allele num: 11450
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

FS
type: SiteQuality
SIO_000300: 2.043e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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SIO_000300: 2.95e0

DP
type: SiteQuality
SIO_000300: 1.648517e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

BaseQRankSum
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SIO_000300: 1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.41e-2

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.522579859313621e-5
allele num: 65678
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

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

Latino
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allele frequency: 2.620087336244541e-4
allele num: 11450
num of homozygotes: 0

African
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

InbreedingCoeff
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QD
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FS
type: SiteQuality
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DP
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ReadPosRankSum
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VQSLOD
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SIO_000300: 2.95e0

MQ
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SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 65958
num of homozygotes: 0

Latino
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South Asian
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Other
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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QD
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 66150
num of homozygotes: 0

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

European (Finnish)
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European (Non-Finnish)
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Other
type: Population
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Latino
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African
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South Asian
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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SIO_000300: -1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.223e0

FS
type: SiteQuality
SIO_000300: 9.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.680717e6

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 4514
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5155
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1446
bin: 8.75e1
variant carriers: 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: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504664459825459e-5
allele num: 66460
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.082e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e0

MQRankSum
type: SiteQuality
SIO_000300: -1.72e-1

DP
type: SiteQuality
SIO_000300: 1.680717e6

FS
type: SiteQuality
SIO_000300: 9.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.223e0

VQSLOD
type: SiteQuality
SIO_000300: -2.183e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3660
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008604609182261e-5
allele num: 66476
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.358e0

FS
type: SiteQuality
SIO_000300: 5.993e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: -1.632e-1

QD
type: SiteQuality
SIO_000300: 1.184e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

DP
type: SiteQuality
SIO_000300: 1.681456e6

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3226
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 40

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.595604775912787e-4
allele num: 11558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 23
allele frequency: 3.458750639116966e-4
allele num: 66498
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.268045259461569e-3
allele num: 10252
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

FS
type: SiteQuality
SIO_000300: 7.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.61e-2

QD
type: SiteQuality
SIO_000300: 1.285e1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

DP
type: SiteQuality
SIO_000300: 1.683965e6

GenotypeQuality
all individuals: 8708
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5162
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4521
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31354
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variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 8.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.746588693957115e-5
allele num: 10260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.001e0

QD
type: SiteQuality
SIO_000300: 1.392e1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.04e-1

DP
type: SiteQuality
SIO_000300: 1.684214e6

GenotypeQuality
all individuals: 8718
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 101
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variant carriers: 0

GenotypeQuality
all individuals: 1840
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.77e0

DP
type: SiteQuality
SIO_000300: 1.68549e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

QD
type: SiteQuality
SIO_000300: 1.253e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1839
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
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: 6594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.258e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 2.8817e1

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

QD
type: SiteQuality
SIO_000300: 9.91e0

DP
type: SiteQuality
SIO_000300: 1.688724e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 50

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 8763
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variant carriers: 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: 20
allele frequency: 3.001290554938624e-4
allele num: 66638
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
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: 30
allele frequency: 4.541326067211626e-3
allele num: 6606
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.331e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.27e0

FS
type: SiteQuality
SIO_000300: 6.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

DP
type: SiteQuality
SIO_000300: 1.693664e6

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3666
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GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
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South Asian
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allele frequency: 6.056201550387597e-5
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European (Non-Finnish)
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allele frequency: 3.000840235265874e-5
allele num: 66648
num of homozygotes: 0

East Asian
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.966e1

DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66660
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African
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Other
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South Asian
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Latino
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QD
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InbreedingCoeff
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BaseQRankSum
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MQ
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MQRankSum
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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African
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

African
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allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

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

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

European (Non-Finnish)
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Other
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South Asian
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East Asian
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Latino
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European (Finnish)
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InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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Other
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South Asian
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African
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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QD
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BaseQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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African
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FS
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QD
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ReadPosRankSum
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VQSLOD
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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Other
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African
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MQRankSum
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MQ
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VQSLOD
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QD
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ClippingRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele num: 11578
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Other
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South Asian
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East Asian
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European (Non-Finnish)
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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DP
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MQ
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FS
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MQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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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 num: 16512
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Latino
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European (Finnish)
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ClippingRankSum
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SIO_000300: -4.39e-1

FS
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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VQSLOD
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BaseQRankSum
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DP
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SIO_000300: 1.696433e6

ReadPosRankSum
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SIO_000300: 4.56e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0.0e0
allele num: 11578
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African
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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allele frequency: 3.00815209216978e-5
allele num: 66486
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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QD
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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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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Other
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Latino
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ReadPosRankSum
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MQRankSum
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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African
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ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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QD
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VQSLOD
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DP
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BaseQRankSum
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Finnish)
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East Asian
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Other
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African
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European (Non-Finnish)
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ClippingRankSum
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FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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MQRankSum
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FS
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VQSLOD
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DP
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MQ
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QD
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European (Non-Finnish)
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East Asian
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South Asian
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African
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MQRankSum
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ReadPosRankSum
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DP
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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African
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FS
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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DP
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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South Asian
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MQRankSum
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MQ
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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DP
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ReadPosRankSum
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GenotypeQuality
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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ReadPosRankSum
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DP
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African
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East Asian
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VQSLOD
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African
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VQSLOD
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SIO_000300: 6.15e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.08e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

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

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.747e0

DP
type: SiteQuality
SIO_000300: 1.704406e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.85e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.19e1

FS
type: SiteQuality
SIO_000300: 5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.15e-1

GenotypeQuality
all individuals: 8807
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.056e0

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.704179e6

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

GenotypeQuality
all individuals: 31855
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1856
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 2.439e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

QD
type: SiteQuality
SIO_000300: 1.385e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.409999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

DP
type: SiteQuality
SIO_000300: 1.704175e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.42e-1

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1461
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8807
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
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

VQSLOD
type: SiteQuality
SIO_000300: -9.068000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.03e0

MQ
type: SiteQuality
SIO_000300: 5.908e1

FS
type: SiteQuality
SIO_000300: 1.895e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.312e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.02e-1

QD
type: SiteQuality
SIO_000300: 1.167e1

DP
type: SiteQuality
SIO_000300: 1.704291e6

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5313
bin: 9.75e1
variant carriers: 65

GenotypeQuality
all individuals: 1852
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 60
allele frequency: 8.990649724286741e-4
allele num: 66736
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: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-1

DP
type: SiteQuality
SIO_000300: 1.709234e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.322e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.18e-1

FS
type: SiteQuality
SIO_000300: 5.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31846
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
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

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 6.51e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.092e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.704461e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.388e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4525
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5265
bin: 9.75e1
variant carriers: 1

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 8654
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.832e1

VQSLOD
type: SiteQuality
SIO_000300: -1.596e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

FS
type: SiteQuality
SIO_000300: 4.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-1

DP
type: SiteQuality
SIO_000300: 1.704288e6

QD
type: SiteQuality
SIO_000300: 1.208e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 5266
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996973057212216e-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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.055e0

FS
type: SiteQuality
SIO_000300: 1.0959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.327e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.68e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.704338e6

QD
type: SiteQuality
SIO_000300: 1.155e1

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8800
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4523
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 3
allele frequency: 2.884060757546626e-4
allele num: 10402
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.756e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

QD
type: SiteQuality
SIO_000300: 1.491e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

DP
type: SiteQuality
SIO_000300: 1.704464e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.69e-1

DP
type: SiteQuality
SIO_000300: 1.704419e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.320000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.044e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.89e-1

FS
type: SiteQuality
SIO_000300: 4.09e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.704281e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 1.734e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.52e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.329e0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.081e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 3653
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variant carriers: 0

GenotypeQuality
all individuals: 31838
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 25
allele frequency: 1.514050387596899e-3
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.544e0

QD
type: SiteQuality
SIO_000300: 1.145e1

DP
type: SiteQuality
SIO_000300: 1.706726e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.807e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3656
bin: 7.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 10
allele frequency: 6.056201550387597e-4
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.254e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

FS
type: SiteQuality
SIO_000300: 1.179e0

DP
type: SiteQuality
SIO_000300: 1.704973e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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: 10400
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 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: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

FS
type: SiteQuality
SIO_000300: 1.092e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.370000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.704082e6

QD
type: SiteQuality
SIO_000300: 1.18e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.139999999999999e-1

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

European (Finnish)
type: Population
allele count: 11
allele frequency: 1.663138796492289e-3
allele num: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 92
allele frequency: 1.378814219770997e-3
allele num: 66724
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.107e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

BaseQRankSum
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.712698e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5273
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GenotypeQuality
all individuals: 10
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

East Asian
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European (Finnish)
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Other
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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VQSLOD
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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African
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East Asian
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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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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQ
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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MQ
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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African
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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DP
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MQ
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VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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African
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Latino
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European (Non-Finnish)
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ClippingRankSum
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InbreedingCoeff
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FS
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MQRankSum
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QD
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MQ
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BaseQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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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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Latino
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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QD
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BaseQRankSum
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ReadPosRankSum
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MQ
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FS
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MQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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South Asian
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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MQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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East Asian
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ReadPosRankSum
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FS
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DP
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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ClippingRankSum
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VQSLOD
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FS
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DP
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MQRankSum
type: SiteQuality
SIO_000300: -6.41e-1

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

GenotypeQuality
all individuals: 358
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5269
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3603
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4456
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1843
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3237
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.519842106849067e-5
allele num: 66374
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.87e0

DP
type: SiteQuality
SIO_000300: 1.678781e6

FS
type: SiteQuality
SIO_000300: 1.421e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

GenotypeQuality
all individuals: 5265
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1846
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1461
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0