SNP Links for Gene (Select 101928440) - SNP

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Select item 14908680631.

rs1490868063 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:33774070 (GRCh38)
11:33795616 (GRCh37)
Canonical SPDI:: NC_000011.10:33774069:A:C
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.33774070A>C, NC_000011.9:g.33795616A>C

Select item 14897760322.

rs1489776032 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:33772985 (GRCh38)
11:33794531 (GRCh37)
Canonical SPDI:: NC_000011.10:33772984:G:T
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000011.10:g.33772985G>T, NC_000011.9:g.33794531G>T

Select item 14895716693.

rs1489571669 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:33775888 (GRCh38)
11:33797434 (GRCh37)
Canonical SPDI:: NC_000011.10:33775887:C:G
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.33775888C>G, NC_000011.9:g.33797434C>G

Select item 14887686404.

rs1488768640 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:33774075 (GRCh38)
11:33795621 (GRCh37)
Canonical SPDI:: NC_000011.10:33774074:G:A
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.33774075G>A, NC_000011.9:g.33795621G>A

Select item 14880045505.

rs1488004550 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:33776007 (GRCh38)
11:33797553 (GRCh37)
Canonical SPDI:: NC_000011.10:33776006:T:C
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.33776007T>C, NC_000011.9:g.33797553T>C

Select item 14866317936.

rs1486631793 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:33774226 (GRCh38)
11:33795772 (GRCh37)
Canonical SPDI:: NC_000011.10:33774225:C:T
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000094/1 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000029/4 (GnomAD)
HGVS:: NC_000011.10:g.33774226C>T, NC_000011.9:g.33795772C>T

Select item 14856940877.

rs1485694087 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:33773103 (GRCh38)
11:33794649 (GRCh37)
Canonical SPDI:: NC_000011.10:33773102:C:A
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.33773103C>A, NC_000011.9:g.33794649C>A

Select item 14847389158.

rs1484738915 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:33775254 (GRCh38)
11:33796800 (GRCh37)
Canonical SPDI:: NC_000011.10:33775253:G:C
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.33775254G>C, NC_000011.9:g.33796800G>C, NR_120550.1:n.54G>C

Select item 14843119949.

rs1484311994 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:33773424 (GRCh38)
11:33794970 (GRCh37)
Canonical SPDI:: NC_000011.10:33773423:A:G
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.33773424A>G, NC_000011.9:g.33794970A>G

Select item 148412761110.

rs1484127611 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:33773184 (GRCh38)
11:33794730 (GRCh37)
Canonical SPDI:: NC_000011.10:33773183:G:C
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.33773184G>C, NC_000011.9:g.33794730G>C

Select item 148324128111.

rs1483241281 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 11:33774685 (GRCh38)
11:33796231 (GRCh37)
Canonical SPDI:: NC_000011.10:33774684:A:C,NC_000011.10:33774684:A:G
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.33774685A>C, NC_000011.10:g.33774685A>G, NC_000011.9:g.33796231A>C, NC_000011.9:g.33796231A>G

Select item 148228084012.

rs1482280840 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:33773114 (GRCh38)
11:33794660 (GRCh37)
Canonical SPDI:: NC_000011.10:33773113:A:G,NC_000011.10:33773113:A:T
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000054/1 (ALFA)
G=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
G=0.000223/1 (Estonian)
HGVS:: NC_000011.10:g.33773114A>G, NC_000011.10:g.33773114A>T, NC_000011.9:g.33794660A>G, NC_000011.9:g.33794660A>T

Select item 148142332913.

rs1481423329 [Homo sapiens]

Variant type:: DELINS
Alleles:: CCT>- [Show Flanks]
Chromosome:: 11:33774817 (GRCh38)
11:33796363 (GRCh37)
Canonical SPDI:: NC_000011.10:33774811:CTCCTCCT:CTCCT
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTCCT=0.000054/1 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000021/3 (GnomAD)
-=0.00006/1 (TOMMO)
-=0.000224/1 (Estonian)
HGVS:: NC_000011.10:g.33774814CCT[1], NC_000011.9:g.33796360CCT[1]

Select item 148064264214.

rs1480642642 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:33775030 (GRCh38)
11:33796576 (GRCh37)
Canonical SPDI:: NC_000011.10:33775029:C:G,NC_000011.10:33775029:C:T
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000011.10:g.33775030C>G, NC_000011.10:g.33775030C>T, NC_000011.9:g.33796576C>G, NC_000011.9:g.33796576C>T

Select item 147944082915.

rs1479440829 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:33773661 (GRCh38)
11:33795207 (GRCh37)
Canonical SPDI:: NC_000011.10:33773660:C:G
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.33773661C>G, NC_000011.9:g.33795207C>G

Select item 147852532116.

rs1478525321 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:33773436 (GRCh38)
11:33794982 (GRCh37)
Canonical SPDI:: NC_000011.10:33773435:A:G
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.33773436A>G, NC_000011.9:g.33794982A>G

Select item 147845789917.

rs1478457899 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:33773159 (GRCh38)
11:33794705 (GRCh37)
Canonical SPDI:: NC_000011.10:33773158:A:G
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.33773159A>G, NC_000011.9:g.33794705A>G

Select item 147621924018.

rs1476219240 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:33774633 (GRCh38)
11:33796179 (GRCh37)
Canonical SPDI:: NC_000011.10:33774632:C:G
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000015/2 (GnomAD)
HGVS:: NC_000011.10:g.33774633C>G, NC_000011.9:g.33796179C>G

Select item 147432631719.

rs1474326317 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 11:33775065 (GRCh38)
11:33796611 (GRCh37)
Canonical SPDI:: NC_000011.10:33775064:A:C,NC_000011.10:33775064:A:G
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.33775065A>C, NC_000011.10:g.33775065A>G, NC_000011.9:g.33796611A>C, NC_000011.9:g.33796611A>G

Select item 147307999120.

rs1473079991 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:33774049 (GRCh38)
11:33795595 (GRCh37)
Canonical SPDI:: NC_000011.10:33774048:C:G
Gene:: FBXO3 (Varview), FBXO3-DT (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.33774049C>G, NC_000011.9:g.33795595C>G

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