Related gene-specific medical variations for Gene (Select 2778) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3374747	NM_000516.7(GNAS):c.124C>G (p.Arg42Gly)	GNAS (R42G)	Single nucleotide variant (missense variant +1 more)	Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, acrodysostosis and osteoma cutis	GLikely pathogenic
Select item 3361782	NM_000516.7(GNAS):c.1117C>T (p.Arg373Cys)	GNAS (R1001C +7 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3361567	NM_016592.5(GNAS):c.536C>G (p.Pro179Arg)	GNAS, GNAS-AS1 (P179R)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 3359296	NM_000516.7(GNAS):c.175C>G (p.Gln59Glu)	GNAS (Q27E +2 more)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance
Select item 3357867	NM_016592.5(GNAS):c.479C>T (p.Thr160Ile)	GNAS, GNAS-AS1 (T160I)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3357812	NM_016592.5(GNAS):c.337_348del (p.111TESE[1])	GNAS, GNAS-AS1	Deletion (5 prime UTR variant)	GNAS-related disorder	GUncertain significance
Select item 3357514	NM_016592.5(GNAS):c.*4A>T	GNAS, GNAS-AS1 (E2V)	Single nucleotide variant (missense variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3357101	NM_016592.5(GNAS):c.3_5delinsAAT (p.Met1_Asp2delinsIleIle)	GNAS, GNAS-AS1	Indel (5 prime UTR variant +2 more)	GNAS-related disorder	GUncertain significance
Select item 3357012	NM_016592.5(GNAS):c.315A>G (p.Glu105=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3356377	NM_016592.5(GNAS):c.536_543dup (p.Thr182fs)	GNAS-AS1, GNAS (T182fs)	Duplication (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3355872	NM_016592.5(GNAS):c.6T>C (p.Asp2=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3355554	NM_016592.5(GNAS):c.466G>A (p.Gly156Ser)	GNAS, GNAS-AS1 (G156S)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3355486	NM_016592.5(GNAS):c.618G>A (p.Glu206=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3354491	NM_016592.5(GNAS):c.41G>A (p.Arg14His)	GNAS, GNAS-AS1 (R14H)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3354321	NM_016592.5(GNAS):c.338_385dup (p.Glu128_Pro129insArgGluThrGluSerGluIleGluSerGluThrAspPheGluThrGlu)	GNAS, GNAS-AS1	Duplication (5 prime UTR variant)	GNAS-related disorder	GUncertain significance
Select item 3353733	NM_016592.5(GNAS):c.240del (p.Glu81fs)	GNAS, GNAS-AS1 (E81fs)	Deletion (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3353165	NM_016592.5(GNAS):c.463T>G (p.Phe155Val)	GNAS, GNAS-AS1 (F155V)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3352851	NM_016592.5(GNAS):c.647G>C (p.Arg216Pro)	GNAS, GNAS-AS1 (R216P)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3352692	NM_016592.5(GNAS):c.320T>G (p.Phe107Cys)	GNAS, GNAS-AS1 (F107C)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3352433	NM_016592.5(GNAS):c.633G>A (p.Lys211=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3352177	NM_016592.5(GNAS):c.264C>G (p.His88Gln)	GNAS, GNAS-AS1 (H88Q)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3352052	NM_016592.5(GNAS):c.73G>A (p.Gly25Ser)	GNAS, GNAS-AS1 (G25S)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3351632	NM_016592.5(GNAS):c.308A>G (p.Tyr103Cys)	GNAS, GNAS-AS1 (Y103C)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3351166	NM_016592.5(GNAS):c.41G>T (p.Arg14Leu)	GNAS, GNAS-AS1 (R14L)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3351162	NM_016592.5(GNAS):c.132C>A (p.Ala44=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3351101	NM_016592.5(GNAS):c.669G>A (p.Lys223=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3351012	NM_016592.5(GNAS):c.693G>C (p.Pro231=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3349654	NM_016592.5(GNAS):c.575A>G (p.Glu192Gly)	GNAS, GNAS-AS1 (E192G)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3349511	NM_016592.5(GNAS):c.114C>T (p.Ser38=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3349359	NM_016592.5(GNAS):c.377A>G (p.Glu126Gly)	GNAS, GNAS-AS1 (E126G)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3348546	NM_016592.5(GNAS):c.245C>G (p.Ser82Trp)	GNAS, GNAS-AS1 (S82W)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3348393	NR_002785.2(GNAS-AS1):n.819+1831C>T	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant)	GNAS-AS1-related condition	GUncertain significance
Select item 3348239	NM_016592.5(GNAS):c.638A>G (p.Glu213Gly)	GNAS, GNAS-AS1 (E213G)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3348138	NM_016592.5(GNAS):c.595A>G (p.Lys199Glu)	GNAS, GNAS-AS1 (K199E)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3347415	NM_016592.5(GNAS):c.485G>A (p.Arg162His)	GNAS, GNAS-AS1 (R162H)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3346842	NM_016592.5(GNAS):c.610C>G (p.Pro204Ala)	GNAS, GNAS-AS1 (P204A)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3346622	NM_016592.5(GNAS):c.288C>T (p.Ser96=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3346446	NM_016592.5(GNAS):c.327C>T (p.Tyr109=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3346132	NM_016592.5(GNAS):c.415A>T (p.Thr139Ser)	GNAS, GNAS-AS1 (T139S)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3346123	NM_016592.5(GNAS):c.322G>C (p.Asp108His)	GNAS, GNAS-AS1 (D108H)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3345781	NM_016592.5(GNAS):c.699C>G (p.Ser233=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3250676	NM_016592.5(GNAS):c.693G>A (p.Pro231=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 3242103	NM_016592.5(GNAS):c.34C>T (p.Arg12Ter)	GNAS, GNAS-AS1 (R12*)	Single nucleotide variant (5 prime UTR variant +1 more)	Pseudopseudohypoparathyroidism	GLikely pathogenic
Select item 3238642	NM_080425.4(GNAS):c.1792C>T (p.Arg598Cys)	GNAS (R598C)	Single nucleotide variant (synonymous variant +2 more)	McCune-Albright syndrome	GUncertain significance
Select item 3237441	NM_016592.5(GNAS):c.536C>T (p.Pro179Leu)	GNAS, GNAS-AS1 (P179L)	Single nucleotide variant (5 prime UTR variant +1 more)	Pseudopseudohypoparathyroidism	GUncertain significance
Select item 3068317	NM_080425.4(GNAS):c.344G>A (p.Trp115Ter)	GNAS (G53S +1 more)	Single nucleotide variant (missense variant +2 more)	Pseudohypoparathyroidism type I A	GLikely pathogenic
Select item 3065653	NM_080425.4(GNAS):c.648del (p.Gly215_Tyr216insTer)	GNAS (T154fs)	Deletion (frameshift variant +2 more)	Pseudohypoparathyroidism type 1B	GLikely pathogenic
Select item 3059708	NM_016592.5(GNAS):c.570A>G (p.Glu190=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3051457	NM_016592.5(GNAS):c.126C>T (p.Leu42=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3051301	NM_016592.5(GNAS):c.685G>C (p.Ala229Pro)	GNAS, GNAS-AS1 (A229P)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3049774	NM_016592.5(GNAS):c.366G>C (p.Glu122Asp)	GNAS, GNAS-AS1 (E122D)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3048767	NM_016592.5(GNAS):c.589G>A (p.Glu197Lys)	GNAS, GNAS-AS1 (E197K)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3048537	NM_016592.5(GNAS):c.375C>T (p.Phe125=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3047129	NM_016592.5(GNAS):c.592G>A (p.Asp198Asn)	GNAS, GNAS-AS1 (D198N)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 3045751	NM_016592.5(GNAS):c.505C>T (p.Arg169Ter)	GNAS, GNAS-AS1 (R169*)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3043786	NM_016592.5(GNAS):c.417C>A (p.Thr139=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3043388	NM_016592.5(GNAS):c.506G>A (p.Arg169Gln)	GNAS, GNAS-AS1 (R169Q)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3039289	NM_016592.5(GNAS):c.266A>G (p.Glu89Gly)	GNAS, GNAS-AS1 (E89G)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3038893	NM_016592.5(GNAS):c.309C>T (p.Tyr103=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3036067	NM_016592.5(GNAS):c.453G>A (p.Lys151=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3035668	NM_016592.5(GNAS):c.639G>A (p.Glu213=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 3035607	NM_016592.5(GNAS):c.206A>T (p.His69Leu)	GNAS, GNAS-AS1 (H69L)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3032975	NM_016592.5(GNAS):c.729G>A (p.Arg243=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3031307	NM_016592.5(GNAS):c.286T>G (p.Ser96Ala)	GNAS-AS1, GNAS (S96A)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3030494	NM_016592.5(GNAS):c.366G>A (p.Glu122=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3030466	NM_016592.5(GNAS):c.27G>A (p.Gln9=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3030053	NM_016592.5(GNAS):c.642G>T (p.Lys214Asn)	GNAS, GNAS-AS1 (K214N)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3029991	NM_016592.5(GNAS):c.23A>C (p.Gln8Pro)	GNAS, GNAS-AS1 (Q8P)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3029819	NM_016592.5(GNAS):c.369C>A (p.Thr123=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3029386	NM_016592.5(GNAS):c.621G>A (p.Ser207=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3029342	NM_016592.5(GNAS):c.511C>T (p.Pro171Ser)	GNAS, GNAS-AS1 (P171S)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 3029235	NM_016592.5(GNAS):c.303A>G (p.Leu101=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GLikely benign
Select item 3024406	NM_016592.5(GNAS):c.713G>A (p.Gly238Glu)	GNAS, GNAS-AS1 (G238E)	Single nucleotide variant (5 prime UTR variant +1 more)	Duane retraction syndrome	GUncertain significance
Select item 3024405	NM_016592.5(GNAS):c.304G>C (p.Glu102Gln)	GNAS, GNAS-AS1 (E102Q)	Single nucleotide variant (5 prime UTR variant +1 more)	Duane retraction syndrome	GUncertain significance
Select item 2672880	NM_016592.5(GNAS):c.531C>G (p.Arg177=)	GNAS, GNAS-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2672103	NM_000516.7(GNAS):c.380G>C (p.Arg127Thr)	GNAS (R112T +7 more)	Single nucleotide variant (missense variant +1 more)	Pseudohypoparathyroidism type I A	GUncertain significance
Select item 2671935	NM_000516.7(GNAS):c.320T>G (p.Val107Gly)	GNAS (V107G +7 more)	Single nucleotide variant (missense variant +1 more)	Pseudopseudohypoparathyroidism	GLikely pathogenic
Select item 2664039	NM_000516.7(GNAS):c.967G>C (p.Asp323His)	GNAS (D264H +7 more)	Single nucleotide variant (missense variant +1 more)	Pseudohypoparathyroidism type I A	GUncertain significance
Select item 2662210	NM_016592.5(GNAS):c.354_383del (p.Ile119_Glu128del)	GNAS, GNAS-AS1	Deletion (5 prime UTR variant)	not provided	GUncertain significance
Select item 2652450	NM_000516.7(GNAS):c.531-1143G>A	GNAS, LOC130066270	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2652449	NM_000516.7(GNAS):c.531-1162A>C	GNAS, LOC130066270	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2652447	NM_080425.4(GNAS):c.2069-4915C>T	GNAS, LOC130066266	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2652437	NM_016592.5(GNAS):c.*42+10000C>T	GNAS-AS1, GNAS	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2652436	NM_016592.5(GNAS):c.*42+9924G>A	GNAS, GNAS-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2652435	NM_016592.5(GNAS):c.364G>A (p.Glu122Lys)	GNAS, GNAS-AS1 (E122K)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2652434	NM_016592.5(GNAS):c.334G>C (p.Glu112Gln)	GNAS, GNAS-AS1 (E112Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2636584	NM_016592.5(GNAS):c.44A>G (p.His15Arg)	GNAS, GNAS-AS1 (H15R)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 2636041	NM_016592.5(GNAS):c.398C>T (p.Pro133Leu)	GNAS, GNAS-AS1 (P133L)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 2634429	NM_016592.5(GNAS):c.631A>G (p.Lys211Glu)	GNAS, GNAS-AS1 (K211E)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 2634213	NM_016592.5(GNAS):c.701C>T (p.Pro234Leu)	GNAS, GNAS-AS1 (P234L)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 2634184	NM_016592.5(GNAS):c.634GAG[1] (p.Glu213del)	GNAS, GNAS-AS1 (E213del)	Microsatellite (5 prime UTR variant)	GNAS-related disorder	GUncertain significance
Select item 2634122	NM_016592.5(GNAS):c.412G>A (p.Glu138Lys)	GNAS, GNAS-AS1 (E138K)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 2633317	NM_016592.5(GNAS):c.72A>G (p.Ile24Met)	GNAS, GNAS-AS1 (I24M)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 2631688	NM_016592.5(GNAS):c.713G>T (p.Gly238Val)	GNAS, GNAS-AS1 (G238V)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 2631479	NM_016592.5(GNAS):c.611C>T (p.Pro204Leu)	GNAS, GNAS-AS1 (P204L)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 2630439	NM_016592.5(GNAS):c.720C>G (p.Ile240Met)	GNAS, GNAS-AS1 (I240M)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 2628591	NM_016592.5(GNAS):c.127C>T (p.Arg43Cys)	GNAS, GNAS-AS1 (R43C)	Single nucleotide variant (5 prime UTR variant +1 more)	GNAS-related disorder	GUncertain significance
Select item 2627910	NM_000516.7(GNAS):c.819C>G (p.Phe273Leu)	GNAS (F214L +7 more)	Single nucleotide variant (missense variant +1 more)	Disorders of GNAS Inactivation	GLikely pathogenic
Select item 2584551	NM_080425.4(GNAS):c.1999A>G (p.Lys667Glu)	GNAS (K667E)	Single nucleotide variant (synonymous variant +2 more)	Pseudohypoparathyroidism type 1C +3 more	GUncertain significance
Select item 2582341	NM_000516.7(GNAS):c.847C>T (p.Arg283Cys)	GNAS (R224C +7 more)	Single nucleotide variant (missense variant +1 more)	Pseudopseudohypoparathyroidism	GUncertain significance

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