ClinVar Miner

List of variants in gene CRAT reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_000755.5(CRAT):c.329A>G (p.Tyr110Cys) rs141970897 0.00076
NM_000755.5(CRAT):c.984+20C>T rs372350603 0.00060
NM_000755.5(CRAT):c.612C>T (p.Thr204=) rs144494071 0.00041
NM_000755.5(CRAT):c.1464G>A (p.Thr488=) rs149498107 0.00037
NM_000755.5(CRAT):c.1785C>T (p.Cys595=) rs201995132 0.00025
NM_000755.5(CRAT):c.805+15C>T rs190368307 0.00019
NM_000755.5(CRAT):c.894C>T (p.Asp298=) rs146073229 0.00019
NM_000755.5(CRAT):c.1023C>T (p.Tyr341=) rs376776814 0.00014
NM_000755.5(CRAT):c.27+11C>T rs373031416 0.00011
NM_000755.5(CRAT):c.1764C>T (p.Ser588=) rs764803862 0.00010
NM_000755.5(CRAT):c.738G>A (p.Glu246=) rs141150285 0.00007
NM_000755.5(CRAT):c.1479G>A (p.Val493=) rs770900300 0.00006
NM_000755.5(CRAT):c.879C>T (p.Pro293=) rs528068632 0.00006
NM_000755.5(CRAT):c.805+17G>A rs753767546 0.00004
NM_000755.5(CRAT):c.1036G>A (p.Ala346Thr) rs200277103 0.00001
NM_000755.5(CRAT):c.1205+17G>A rs769855775 0.00001
NM_000755.5(CRAT):c.1206-18C>G rs1286723142 0.00001
NM_000755.5(CRAT):c.1368C>T (p.Ser456=) rs1480535546 0.00001
NM_000755.5(CRAT):c.1458C>T (p.Ser486=) rs775405756 0.00001
NM_000755.5(CRAT):c.1557C>T (p.His519=) rs567099132 0.00001
NM_000755.5(CRAT):c.1665+18G>A rs763608596 0.00001
NM_000755.5(CRAT):c.1666-8G>A rs564235066 0.00001
NM_000755.5(CRAT):c.1770G>A (p.Ser590=) rs762335495 0.00001
NM_000755.5(CRAT):c.1020G>C (p.Val340=)
NM_000755.5(CRAT):c.1038G>A (p.Ala346=)
NM_000755.5(CRAT):c.1044G>A (p.Gly348=)
NM_000755.5(CRAT):c.1077C>T (p.Ile359=)
NM_000755.5(CRAT):c.1086-13G>A
NM_000755.5(CRAT):c.1086-15C>G
NM_000755.5(CRAT):c.1086-17C>T
NM_000755.5(CRAT):c.1086-19G>A
NM_000755.5(CRAT):c.1116G>C (p.Leu372=)
NM_000755.5(CRAT):c.1206-13C>T
NM_000755.5(CRAT):c.1206-7C>A
NM_000755.5(CRAT):c.1245C>T (p.His415=)
NM_000755.5(CRAT):c.1287A>G (p.Pro429=)
NM_000755.5(CRAT):c.1374C>T (p.Arg458=)
NM_000755.5(CRAT):c.1410G>A (p.Ser470=)
NM_000755.5(CRAT):c.1428C>G (p.Leu476=) rs767455192
NM_000755.5(CRAT):c.1464+17G>A
NM_000755.5(CRAT):c.1464+18A>G
NM_000755.5(CRAT):c.1465-8C>T
NM_000755.5(CRAT):c.1515C>G (p.Gly505=)
NM_000755.5(CRAT):c.1527+13G>A rs759318673
NM_000755.5(CRAT):c.1536C>T (p.Arg512=)
NM_000755.5(CRAT):c.153G>A (p.Leu51=)
NM_000755.5(CRAT):c.1567C>T (p.Leu523=)
NM_000755.5(CRAT):c.1575G>T (p.Leu525=)
NM_000755.5(CRAT):c.1584C>T (p.Ile528=)
NM_000755.5(CRAT):c.159G>A (p.Ala53=)
NM_000755.5(CRAT):c.1644C>T (p.His548=)
NM_000755.5(CRAT):c.1704C>T (p.Pro568=)
NM_000755.5(CRAT):c.1710C>G (p.Val570=)
NM_000755.5(CRAT):c.1716C>T (p.Asp572=)
NM_000755.5(CRAT):c.1734T>C (p.Tyr578=)
NM_000755.5(CRAT):c.1830G>C (p.Ala610=)
NM_000755.5(CRAT):c.183G>A (p.Glu61=)
NM_000755.5(CRAT):c.231A>G (p.Gly77=)
NM_000755.5(CRAT):c.27+18C>G
NM_000755.5(CRAT):c.27+18C>T
NM_000755.5(CRAT):c.291+13A>G
NM_000755.5(CRAT):c.291+19A>C
NM_000755.5(CRAT):c.318C>T (p.Ala106=)
NM_000755.5(CRAT):c.354G>A (p.Ser118=)
NM_000755.5(CRAT):c.354G>T (p.Ser118=)
NM_000755.5(CRAT):c.387C>T (p.Phe129=)
NM_000755.5(CRAT):c.402T>A (p.Gly134=)
NM_000755.5(CRAT):c.410+12G>A
NM_000755.5(CRAT):c.411-20T>C rs113134387
NM_000755.5(CRAT):c.465-15C>G
NM_000755.5(CRAT):c.477C>T (p.Pro159=)
NM_000755.5(CRAT):c.489G>C (p.Leu163=) rs758982074
NM_000755.5(CRAT):c.549G>A (p.Pro183=)
NM_000755.5(CRAT):c.630+17C>G
NM_000755.5(CRAT):c.631-12G>A
NM_000755.5(CRAT):c.660C>T (p.Asp220=)
NM_000755.5(CRAT):c.756C>T (p.Thr252=)
NM_000755.5(CRAT):c.805+8T>C
NM_000755.5(CRAT):c.806-16C>T
NM_000755.5(CRAT):c.806-18G>C
NM_000755.5(CRAT):c.825C>T (p.Ser275=)
NM_000755.5(CRAT):c.840G>A (p.Gln280=)
NM_000755.5(CRAT):c.84C>T (p.Phe28=)
NM_000755.5(CRAT):c.855C>T (p.Thr285=)
NM_000755.5(CRAT):c.984+10G>A
NM_000755.5(CRAT):c.984+15G>A
NM_000755.5(CRAT):c.985-14C>T
NM_000755.5(CRAT):c.9C>T (p.Ala3=)

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