GGA3[gene] and "single gene"[properties] - ClinVar

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Items: 56

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2302743	NM_138619.4(GGA3):c.2162G>A (p.Gly721Glu)	GGA3 (G688E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595688	NM_138619.4(GGA3):c.2128G>A (p.Glu710Lys)	GGA3 (E638K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234505	NM_138619.4(GGA3):c.2060A>C (p.Lys687Thr)	GGA3 (K615T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281292	NM_138619.4(GGA3):c.2015C>T (p.Pro672Leu)	GGA3 (P550L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313694	NM_138619.4(GGA3):c.2008A>C (p.Ile670Leu)	GGA3 (I548L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775389	NM_138619.4(GGA3):c.1966T>C (p.Leu656=)	GGA3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3281291	NM_138619.4(GGA3):c.1919A>G (p.Lys640Arg)	GGA3 (K607R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099574	NM_138619.4(GGA3):c.1880T>C (p.Val627Ala)	GGA3 (V505A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516876	NM_138619.4(GGA3):c.1862G>A (p.Arg621Gln)	GGA3 (R499Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286531	NM_138619.4(GGA3):c.1846G>C (p.Glu616Gln)	GGA3 (E583Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343081	NM_138619.4(GGA3):c.1807G>A (p.Asp603Asn)	GGA3 (D481N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495844	NM_138619.4(GGA3):c.1789C>T (p.Leu597Phe)	GGA3 (L475F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306824	NM_138619.4(GGA3):c.1724A>G (p.Lys575Arg)	GGA3 (K503R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341398	NM_138619.4(GGA3):c.1720C>G (p.Pro574Ala)	GGA3 (P541A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099572	NM_138619.4(GGA3):c.1698T>A (p.Ser566Arg)	GGA3 (S494R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281297	NM_138619.4(GGA3):c.1664C>T (p.Thr555Met)	GGA3 (T433M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494659	NM_138619.4(GGA3):c.1639G>A (p.Ala547Thr)	GGA3 (A425T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330836	NM_138619.4(GGA3):c.1618C>G (p.Leu540Val)	GGA3 (L468V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099571	NM_138619.4(GGA3):c.1562A>G (p.Gln521Arg)	GGA3 (Q399R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229758	NM_138619.4(GGA3):c.1534G>A (p.Ala512Thr)	GGA3 (A390T +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3099570	NM_138619.4(GGA3):c.1525G>C (p.Gly509Arg)	GGA3 (G387R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529261	NM_138619.4(GGA3):c.1519G>A (p.Ala507Thr)	GGA3 (A385T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099569	NM_138619.4(GGA3):c.1472C>T (p.Ala491Val)	GGA3 (A419V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390221	NM_138619.4(GGA3):c.1436C>T (p.Ala479Val)	GGA3 (A357V +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3099568	NM_138619.4(GGA3):c.1420G>A (p.Val474Ile)	GGA3 (V352I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383095	NM_138619.4(GGA3):c.1390C>T (p.Pro464Ser)	GGA3 (P392S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606936	NM_138619.4(GGA3):c.1366A>G (p.Ser456Gly)	GGA3 (S334G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284583	NM_138619.4(GGA3):c.1337T>C (p.Leu446Pro)	GGA3 (L413P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557937	NM_138619.4(GGA3):c.1286T>A (p.Phe429Tyr)	GGA3 (F396Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555061	NM_138619.4(GGA3):c.1285T>G (p.Phe429Val)	GGA3 (F357V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469012	NM_138619.4(GGA3):c.1278C>G (p.Asp426Glu)	GGA3 (D354E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281290	NM_138619.4(GGA3):c.1276G>A (p.Asp426Asn)	GGA3 (D393N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356283	NM_138619.4(GGA3):c.1258C>T (p.Leu420Phe)	GGA3 (L348F +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3099582	NM_138619.4(GGA3):c.993G>C (p.Glu331Asp)	GGA3 (E259D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099581	NM_138619.4(GGA3):c.952A>G (p.Ser318Gly)	GGA3 (S196G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400893	NM_138619.4(GGA3):c.869T>C (p.Ile290Thr)	GGA3 (I168T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099580	NM_138619.4(GGA3):c.800G>A (p.Ser267Asn)	GGA3 (S145N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261416	NM_138619.4(GGA3):c.796G>A (p.Ala266Thr)	GGA3 (A233T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224020	NM_138619.4(GGA3):c.778C>T (p.Arg260Trp)	GGA3 (R188W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404221	NM_138619.4(GGA3):c.737A>T (p.Glu246Val)	GGA3 (E124V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099579	NM_138619.4(GGA3):c.734G>A (p.Arg245Lys)	GGA3 (R212K +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2255700	NM_138619.4(GGA3):c.703T>C (p.Tyr235His)	GGA3 (Y202H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2648250	NM_138619.4(GGA3):c.656A>G (p.Glu219Gly)	GGA3 (E147G +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2389985	NM_138619.4(GGA3):c.485C>G (p.Pro162Arg)	GGA3 (P162R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099578	NM_138619.4(GGA3):c.479C>T (p.Pro160Leu)	GGA3 (P88L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281295	NM_138619.4(GGA3):c.467T>A (p.Leu156Gln)	GGA3 (L34Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601629	NM_138619.4(GGA3):c.409A>G (p.Met137Val)	GGA3 (M137V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257144	NM_138619.4(GGA3):c.356A>T (p.Tyr119Phe)	GGA3 (Y47F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3099577	NM_138619.4(GGA3):c.265T>C (p.Phe89Leu)	GGA3 (F17L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3099576	NM_138619.4(GGA3):c.263G>A (p.Arg88His)	GGA3 (R88H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3099575	NM_138619.4(GGA3):c.256A>G (p.Lys86Glu)	GGA3 (K14E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3281294	NM_138619.4(GGA3):c.247G>A (p.Glu83Lys)	GGA3 (E11K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302244	NM_138619.4(GGA3):c.182A>G (p.Glu61Gly)	GGA3 (E61G)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2405790	NM_138619.4(GGA3):c.159G>T (p.Lys53Asn)	GGA3 (K53N)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 712747	NM_138619.4(GGA3):c.105G>A (p.Gln35=)	GGA3	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GBenign
Select item 3099567	NM_138619.4(GGA3):c.11C>T (p.Ala4Val)	GGA3 (A4V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance

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Items: 56