ClinVar Miner

List of variants in gene FRAS1 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NM_025074.7(FRAS1):c.*1301G>A rs3210826
NM_025074.7(FRAS1):c.*1814G>A rs17003321
NM_025074.7(FRAS1):c.*1995G>T rs72873318
NM_025074.7(FRAS1):c.*2154C>T rs3811747
NM_025074.7(FRAS1):c.*2489T>C rs11098227
NM_025074.7(FRAS1):c.*2700G>A rs11098228
NM_025074.7(FRAS1):c.*2824_*2825insTTTT rs397724155
NM_025074.7(FRAS1):c.*282A>T rs3749485
NM_025074.7(FRAS1):c.*33T>A rs72659058
NM_025074.7(FRAS1):c.*518dup rs397752464
NM_025074.7(FRAS1):c.-65T>C rs6832285
NM_025074.7(FRAS1):c.10377C>T (p.Thr3459=) rs3749487
NM_025074.7(FRAS1):c.10648+25del rs397994139
NM_025074.7(FRAS1):c.10696G>A (p.Val3566Ile) rs931606
NM_025074.7(FRAS1):c.108+2546T>C rs10008489
NM_025074.7(FRAS1):c.10877T>C (p.Val3626Ala) rs34670941
NM_025074.7(FRAS1):c.11037C>G (p.Pro3679=) rs4975070
NM_025074.7(FRAS1):c.11056C>T (p.Leu3686=) rs4975139
NM_025074.7(FRAS1):c.11445+68_11445+69del
NM_025074.7(FRAS1):c.1396T>A (p.Leu466Ile) rs12504081
NM_025074.7(FRAS1):c.1617A>G (p.Arg539=) rs345528
NM_025074.7(FRAS1):c.1947T>C (p.His649=) rs345514
NM_025074.7(FRAS1):c.2060A>G (p.Asp687Gly) rs345513
NM_025074.7(FRAS1):c.2450C>T (p.Ala817Val) rs6835769
NM_025074.7(FRAS1):c.3068G>A (p.Gly1023Glu) rs17459809
NM_025074.7(FRAS1):c.3124G>A (p.Ala1042Thr) rs114077522
NM_025074.7(FRAS1):c.3151+14_3151+15dup rs398092530
NM_025074.7(FRAS1):c.3312T>C (p.Ser1104=) rs35774552
NM_025074.7(FRAS1):c.3406G>A (p.Glu1136Lys) rs12512164
NM_025074.7(FRAS1):c.5366+13T>G rs2170899
NM_025074.7(FRAS1):c.604-132G>A rs6856362
NM_025074.7(FRAS1):c.604-8G>A rs2867014
NM_025074.7(FRAS1):c.6444C>T (p.Thr2148=) rs17003235
NM_025074.7(FRAS1):c.6468C>T (p.His2156=) rs753752
NM_025074.7(FRAS1):c.7011G>A (p.Ala2337=) rs6851427
NM_025074.7(FRAS1):c.7110C>T (p.His2370=) rs7660664
NM_025074.7(FRAS1):c.7132A>G (p.Lys2378Glu) rs7684722
NM_025074.7(FRAS1):c.7254A>G (p.Lys2418=) rs34840208
NM_025074.7(FRAS1):c.7371+11T>C rs7664505
NM_025074.7(FRAS1):c.8439C>T (p.Asp2813=) rs11098194
NM_025074.7(FRAS1):c.8745C>T (p.Phe2915=) rs41327848
NM_025074.7(FRAS1):c.9116-11T>C rs7677541
NM_025074.7(FRAS1):c.9116-5C>G rs7695038
NM_025074.7(FRAS1):c.95A>G (p.Asp32Gly) rs4859905
NM_025074.7(FRAS1):c.9808A>C (p.Arg3270=) rs3749488

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