"Ambry Genetics"[submitter] AND "PRKAR1A"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1981237	NM_001267727.2(ARSG):c.1310C>T (p.Ala437Val)	ARSG, PRKAR1A (A436V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1002055	NM_001267727.2(ARSG):c.1412G>A (p.Gly471Asp)	ARSG, PRKAR1A (G470D +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1375874	NM_001267727.2(ARSG):c.1418C>T (p.Ala473Val)	PRKAR1A, ARSG (A472V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1524091	NM_001267727.2(ARSG):c.1501G>A (p.Ala501Thr)	ARSG, PRKAR1A (A500T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2068129	NM_001267727.2(ARSG):c.1574C>T (p.Ala525Val)	ARSG, PRKAR1A (A524V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3190574	NM_017983.7(WIPI1):c.1322G>A (p.Gly441Asp)	ARSG, PRKAR1A +1 more (G441D +1 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2617959	NM_017983.7(WIPI1):c.1220G>A (p.Arg407Gln)	ARSG, PRKAR1A +1 more (R407Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2519721	NM_017983.7(WIPI1):c.1214C>T (p.Ala405Val)	ARSG, PRKAR1A +1 more (A323V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2513367	NM_017983.7(WIPI1):c.1184C>T (p.Thr395Met)	ARSG, PRKAR1A +1 more (T313M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3190573	NM_017983.7(WIPI1):c.1094C>G (p.Thr365Arg)	ARSG, PRKAR1A +1 more (T283R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2326954	NM_017983.7(WIPI1):c.1069C>T (p.His357Tyr)	ARSG, PRKAR1A +1 more (H275Y +1 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2299575	NM_017983.7(WIPI1):c.1046G>A (p.Gly349Glu)	ARSG, PRKAR1A +1 more (G267E +1 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2544480	NM_017983.7(WIPI1):c.950T>A (p.Ile317Asn)	ARSG, PRKAR1A +1 more (I317N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2225566	NM_017983.7(WIPI1):c.922C>T (p.Arg308Cys)	ARSG, PRKAR1A +1 more (R226C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2255928	NM_017983.7(WIPI1):c.917C>T (p.Thr306Ile)	ARSG, PRKAR1A +1 more (T224I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2588786	NM_017983.7(WIPI1):c.847T>C (p.Phe283Leu)	ARSG, PRKAR1A +1 more (F201L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2325263	NM_017983.7(WIPI1):c.832T>A (p.Tyr278Asn)	ARSG, PRKAR1A +1 more (Y278N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2300421	NM_017983.7(WIPI1):c.793A>G (p.Thr265Ala)	ARSG, PRKAR1A +1 more (T183A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2393222	NM_017983.7(WIPI1):c.760G>A (p.Glu254Lys)	ARSG, PRKAR1A +1 more (E254K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2249374	NM_017983.7(WIPI1):c.649C>G (p.Pro217Ala)	ARSG, PRKAR1A +1 more (P217A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2280776	NM_017983.7(WIPI1):c.616G>A (p.Glu206Lys)	ARSG, PRKAR1A +1 more (E206K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3190578	NM_017983.7(WIPI1):c.556G>A (p.Glu186Lys)	ARSG, PRKAR1A +1 more (E104K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2515115	NM_017983.7(WIPI1):c.473C>T (p.Ala158Val)	ARSG, PRKAR1A +1 more (A76V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3190577	NM_017983.7(WIPI1):c.187G>A (p.Val63Met)	ARSG, PRKAR1A +1 more (V63M)	Single nucleotide variant (3 prime UTR variant +4 more)	not specified	GUncertain significance
Select item 3190576	NM_017983.7(WIPI1):c.175G>T (p.Asp59Tyr)	ARSG, PRKAR1A +1 more (D59Y)	Single nucleotide variant (3 prime UTR variant +4 more)	not specified	GUncertain significance
Select item 3190575	NM_017983.7(WIPI1):c.154C>T (p.His52Tyr)	PRKAR1A, WIPI1 (H52Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 1750999	NM_002734.5(PRKAR1A):c.-5G>A	PRKAR1A	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1798648	NM_002734.5(PRKAR1A):c.-2C>A	PRKAR1A	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3222769	NM_002734.5(PRKAR1A):c.3G>A (p.Met1Ile)	PRKAR1A (M1I)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely pathogenic
Select item 2562679	NM_002734.5(PRKAR1A):c.6_11del (p.Glu2_Gly4delinsAsp)	PRKAR1A	Deletion (inframe_indel)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3222775	NM_002734.5(PRKAR1A):c.7T>C (p.Ser3Pro)	PRKAR1A (S3P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3222779	NM_002734.5(PRKAR1A):c.8C>T (p.Ser3Phe)	PRKAR1A (S3F)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1769335	NM_002734.5(PRKAR1A):c.12C>A (p.Gly4=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 819119	NM_002734.5(PRKAR1A):c.13A>G (p.Ser5Gly)	PRKAR1A (S5G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 469058	NM_002734.5(PRKAR1A):c.18C>T (p.Thr6=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Carney complex, type 1 +2 more	GLikely benign
Select item 486163	NM_002734.5(PRKAR1A):c.19G>A (p.Ala7Thr)	PRKAR1A (A7T)	Single nucleotide variant (missense variant)	Carney complex, type 1 +3 more	GConflicting classifications of pathogenicity
Select item 1110806	NM_002734.5(PRKAR1A):c.21C>T (p.Ala7=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Carney complex, type 1 +1 more	GLikely benign
Select item 820883	NM_002734.5(PRKAR1A):c.21C>A (p.Ala7=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Carney complex, type 1 +1 more	GLikely benign
Select item 949669	NM_002734.5(PRKAR1A):c.22G>A (p.Ala8Thr)	PRKAR1A (A8T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 821373	NM_002734.5(PRKAR1A):c.24C>T (p.Ala8=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Carney complex, type 1 +1 more	GLikely benign
Select item 821550	NM_002734.5(PRKAR1A):c.25A>C (p.Ser9Arg)	PRKAR1A (S9R)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 638955	NM_002734.5(PRKAR1A):c.25A>G (p.Ser9Gly)	PRKAR1A (S9G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GUncertain significance
Select item 633376	NM_002734.5(PRKAR1A):c.27T>G (p.Ser9Arg)	PRKAR1A (S9R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 892466	NM_002734.5(PRKAR1A):c.28G>A (p.Glu10Lys)	PRKAR1A (E10K)	Single nucleotide variant (missense variant)	Acrodysostosis 1 with or without hormone resistance +2 more	GUncertain significance
Select item 1001650	NM_002734.5(PRKAR1A):c.33G>C (p.Glu11Asp)	PRKAR1A (E11D)	Single nucleotide variant (missense variant)	Carney complex, type 1 +1 more	GUncertain significance
Select item 660751	NM_002734.5(PRKAR1A):c.35C>G (p.Ala12Gly)	PRKAR1A (A12G)	Single nucleotide variant (missense variant)	Carney complex, type 1 +2 more	GUncertain significance
Select item 952943	NM_002734.5(PRKAR1A):c.37C>T (p.Arg13Cys)	PRKAR1A (R13C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1394679	NM_002734.5(PRKAR1A):c.38G>A (p.Arg13His)	PRKAR1A (R13H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1736854	NM_002734.5(PRKAR1A):c.39C>G (p.Arg13=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1140064	NM_002734.5(PRKAR1A):c.42C>T (p.Ser14=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 1058245	NM_002734.5(PRKAR1A):c.43C>A (p.Leu15Ile)	PRKAR1A (L15I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1741043	NM_002734.5(PRKAR1A):c.44T>C (p.Leu15Pro)	PRKAR1A (L15P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2166733	NM_002734.5(PRKAR1A):c.46C>G (p.Arg16Gly)	PRKAR1A (R16G)	Single nucleotide variant (missense variant)	Carney complex, type 1 +1 more	GUncertain significance
Select item 1038126	NM_002734.5(PRKAR1A):c.47G>A (p.Arg16Gln)	PRKAR1A (R16Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 825535	NM_002734.5(PRKAR1A):c.51A>T (p.Glu17Asp)	PRKAR1A (E17D)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 1567353	NM_002734.5(PRKAR1A):c.57G>A (p.Glu19=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2707745	NM_002734.5(PRKAR1A):c.58C>A (p.Leu20Ile)	PRKAR1A (L20I)	Single nucleotide variant (missense variant)	Carney complex, type 1 +1 more	GUncertain significance
Select item 826111	NM_002734.5(PRKAR1A):c.59T>G (p.Leu20Arg)	PRKAR1A (L20R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1123531	NM_002734.5(PRKAR1A):c.60C>T (p.Leu20=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Carney complex, type 1 +1 more	GLikely benign
Select item 469070	NM_002734.5(PRKAR1A):c.60C>G (p.Leu20=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Carney complex, type 1 +3 more	GLikely benign
Select item 1313482	NM_002734.5(PRKAR1A):c.62A>G (p.Tyr21Cys)	PRKAR1A (Y21C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 469072	NM_002734.5(PRKAR1A):c.63C>T (p.Tyr21=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 958146	NM_002734.5(PRKAR1A):c.64G>A (p.Val22Ile)	PRKAR1A (V22I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 406172	NM_002734.5(PRKAR1A):c.71A>G (p.Lys24Arg)	PRKAR1A (K24R)	Single nucleotide variant (missense variant)	Acrodysostosis 1 with or without hormone resistance +2 more	GUncertain significance
Select item 486157	NM_002734.5(PRKAR1A):c.72G>A (p.Lys24=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Carney complex, type 1 +1 more	GLikely benign
Select item 661103	NM_002734.5(PRKAR1A):c.73C>T (p.His25Tyr)	PRKAR1A (H25Y)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 3222773	NM_002734.5(PRKAR1A):c.75T>G (p.His25Gln)	PRKAR1A (H25Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1092131	NM_002734.5(PRKAR1A):c.75T>C (p.His25=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Carney complex, type 1 +1 more	GLikely benign
Select item 1427404	NM_002734.5(PRKAR1A):c.76A>G (p.Asn26Asp)	PRKAR1A (N26D)	Single nucleotide variant (missense variant)	Carney complex, type 1 +1 more	GUncertain significance
Select item 1761559	NM_002734.5(PRKAR1A):c.79A>G (p.Ile27Val)	PRKAR1A (I27V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 770832	NM_002734.5(PRKAR1A):c.81T>C (p.Ile27=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 486162	NM_002734.5(PRKAR1A):c.81T>G (p.Ile27Met)	PRKAR1A (I27M)	Single nucleotide variant (missense variant)	Carney complex, type 1 +1 more	GUncertain significance
Select item 954235	NM_002734.5(PRKAR1A):c.82C>G (p.Gln28Glu)	PRKAR1A (Q28E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 822384	NM_002734.5(PRKAR1A):c.83A>C (p.Gln28Pro)	PRKAR1A (Q28P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1764009	NM_002734.5(PRKAR1A):c.85G>C (p.Ala29Pro)	PRKAR1A (A29P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 656267	NM_002734.5(PRKAR1A):c.86C>T (p.Ala29Val)	PRKAR1A (A29V)	Single nucleotide variant (missense variant)	Carney complex, type 1 +1 more	GUncertain significance
Select item 41047	NM_002734.5(PRKAR1A):c.87G>A (p.Ala29=)	PRKAR1A	Single nucleotide variant (synonymous variant)	not specified +6 more	GBenign/Likely benign
Select item 1766814	NM_002734.5(PRKAR1A):c.93C>G (p.Leu31=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 469080	NM_002734.5(PRKAR1A):c.94A>G (p.Lys32Glu)	PRKAR1A (K32E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1767509	NM_002734.5(PRKAR1A):c.95A>G (p.Lys32Arg)	PRKAR1A (K32R)	Single nucleotide variant (missense variant)	Carney complex, type 1 +1 more	GUncertain significance
Select item 1767865	NM_002734.5(PRKAR1A):c.96A>G (p.Lys32=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1518964	NM_002734.5(PRKAR1A):c.97G>A (p.Asp33Asn)	PRKAR1A (D33N)	Single nucleotide variant (missense variant)	Carney complex, type 1 +1 more	GUncertain significance
Select item 581188	NM_002734.5(PRKAR1A):c.101C>G (p.Ser34Cys)	PRKAR1A (S34C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 324781	NM_002734.5(PRKAR1A):c.103A>G (p.Ile35Val)	PRKAR1A (I35V)	Single nucleotide variant (missense variant)	Acrodysostosis 1 with or without hormone resistance +3 more	GConflicting classifications of pathogenicity
Select item 1780030	NM_002734.5(PRKAR1A):c.105T>C (p.Ile35=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Carney complex, type 1 +1 more	GLikely benign
Select item 818333	NM_002734.5(PRKAR1A):c.107T>G (p.Val36Gly)	PRKAR1A (V36G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1788991	NM_002734.5(PRKAR1A):c.108G>T (p.Val36=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 486158	NM_002734.5(PRKAR1A):c.108G>C (p.Val36=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1794665	NM_002734.5(PRKAR1A):c.110A>T (p.Gln37Leu)	PRKAR1A (Q37L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1128203	NM_002734.5(PRKAR1A):c.111G>A (p.Gln37=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Carney complex, type 1 +1 more	GLikely benign
Select item 1094136	NM_002734.5(PRKAR1A):c.112T>C (p.Leu38=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1358387	NM_002734.5(PRKAR1A):c.116G>T (p.Cys39Phe)	PRKAR1A (C39F)	Single nucleotide variant (missense variant)	Carney complex, type 1 +1 more	GUncertain significance
Select item 1383406	NM_002734.5(PRKAR1A):c.118A>G (p.Thr40Ala)	PRKAR1A (T40A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 536893	NM_002734.5(PRKAR1A):c.121G>A (p.Ala41Thr)	PRKAR1A (A41T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 3222759	NM_002734.5(PRKAR1A):c.122C>T (p.Ala41Val)	PRKAR1A (A41V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2447619	NM_002734.5(PRKAR1A):c.123T>C (p.Ala41=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1090906	NM_002734.5(PRKAR1A):c.123T>G (p.Ala41=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Carney complex, type 1 +1 more	GLikely benign
Select item 661298	NM_002734.5(PRKAR1A):c.125G>A (p.Arg42Gln)	PRKAR1A (R42Q)	Single nucleotide variant (missense variant)	Acrodysostosis 1 with or without hormone resistance +2 more	GUncertain significance
Select item 837317	NM_002734.5(PRKAR1A):c.127C>T (p.Pro43Ser)	PRKAR1A (P43S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2562687	NM_002734.5(PRKAR1A):c.128C>A (p.Pro43His)	PRKAR1A (P43H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance

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