PRDM15[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3218388	NM_001040424.3(PRDM15):c.3421T>A (p.Tyr1141Asn)	PRDM15 (Y1141N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381441	NM_001040424.3(PRDM15):c.3392C>T (p.Ala1131Val)	PRDM15 (A1197V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218386	NM_001040424.3(PRDM15):c.3313G>A (p.Ala1105Thr)	PRDM15 (A1171T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652684	NM_001040424.3(PRDM15):c.3306G>A (p.Thr1102=)	PRDM15	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3309760	NM_001040424.3(PRDM15):c.3299C>T (p.Pro1100Leu)	PRDM15 (P1100L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652685	NM_001040424.3(PRDM15):c.3246G>A (p.Thr1082=)	PRDM15	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2560500	NM_001040424.3(PRDM15):c.3215C>G (p.Pro1072Arg)	PRDM15 (P1138R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409403	NM_001040424.3(PRDM15):c.3200C>T (p.Pro1067Leu)	PRDM15 (P1067L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218384	NM_001040424.3(PRDM15):c.3197A>T (p.Gln1066Leu)	PRDM15 (Q1086L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218383	NM_001040424.3(PRDM15):c.3032C>T (p.Ala1011Val)	PRDM15 (A223V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527695	NM_001040424.3(PRDM15):c.3010A>T (p.Thr1004Ser)	PRDM15 (T1004S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218382	NM_001040424.3(PRDM15):c.2984C>T (p.Ser995Leu)	PRDM15 (S1061L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2624296	NM_001040424.3(PRDM15):c.2968A>C (p.Asn990His)	PRDM15 (N1010H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309766	NM_001040424.3(PRDM15):c.2924C>T (p.Ala975Val)	PRDM15 (A975V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218381	NM_001040424.3(PRDM15):c.2779G>A (p.Gly927Arg)	PRDM15 (G993R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2227234	NM_001040424.3(PRDM15):c.2767G>A (p.Glu923Lys)	PRDM15 (E989K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309765	NM_001040424.3(PRDM15):c.2728G>A (p.Val910Ile)	PRDM15 (V910I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309764	NM_001040424.3(PRDM15):c.2710G>A (p.Ala904Thr)	PRDM15 (A970T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218380	NM_001040424.3(PRDM15):c.2707G>A (p.Asp903Asn)	PRDM15 (D969N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352869	NM_001040424.3(PRDM15):c.2506G>A (p.Asp836Asn)	PRDM15 (D48N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469386	NM_001040424.3(PRDM15):c.2500G>A (p.Val834Met)	PRDM15 (V46M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652686	NM_001040424.3(PRDM15):c.2496C>T (p.Cys832=)	PRDM15	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2652687	NM_001040424.3(PRDM15):c.2493G>A (p.Thr831=)	PRDM15	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 871179	NM_001040424.3(PRDM15):c.2420G>A (p.Cys807Tyr)	PRDM15 (C827Y +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely pathogenic
Select item 2219060	NM_001040424.3(PRDM15):c.2390C>T (p.Thr797Met)	PRDM15 (T9M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289779	NM_001040424.3(PRDM15):c.2384G>A (p.Arg795Gln)	PRDM15 (R815Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341258	NM_001040424.3(PRDM15):c.2334G>C (p.Glu778Asp)	PRDM15 (E798D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218378	NM_001040424.3(PRDM15):c.2314A>G (p.Lys772Glu)	PRDM15 (K772E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309767	NM_001040424.3(PRDM15):c.2258A>G (p.Lys753Arg)	PRDM15 (K773R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219977	NM_001040424.3(PRDM15):c.2231G>A (p.Arg744His)	PRDM15 (R810H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216745	NM_001040424.3(PRDM15):c.2213G>A (p.Arg738His)	PRDM15 (R758H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309769	NM_001040424.3(PRDM15):c.1721G>A (p.Arg574His)	PRDM15 (R640H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544883	NM_001040424.3(PRDM15):c.1709G>A (p.Arg570His)	PRDM15 (R590H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218375	NM_001040424.3(PRDM15):c.1589G>A (p.Arg530His)	PRDM15 (R596H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380461	NM_001040424.3(PRDM15):c.1588C>T (p.Arg530Cys)	PRDM15 (R550C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509419	NM_001040424.3(PRDM15):c.1579A>G (p.Asn527Asp)	PRDM15 (N527D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408235	NM_001040424.3(PRDM15):c.1544G>A (p.Arg515Gln)	PRDM15 (R515Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2388939	NM_001040424.3(PRDM15):c.1504A>G (p.Met502Val)	PRDM15 (M502V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211262	NM_001040424.3(PRDM15):c.1492C>T (p.Arg498Cys)	PRDM15 (R518C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302500	NM_001040424.3(PRDM15):c.1447G>A (p.Gly483Ser)	PRDM15 (G549S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507717	NM_001040424.3(PRDM15):c.1339G>A (p.Ala447Thr)	PRDM15 (A447T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218374	NM_001040424.3(PRDM15):c.1306G>A (p.Gly436Ser)	PRDM15 (G436S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2478900	NM_001040424.3(PRDM15):c.1228C>T (p.Arg410Cys)	PRDM15 (R410C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218373	NM_001040424.3(PRDM15):c.1213G>A (p.Ala405Thr)	PRDM15 (A405T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2247217	NM_001040424.3(PRDM15):c.1096G>A (p.Gly366Arg)	PRDM15 (G366R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212131	NM_001040424.3(PRDM15):c.1096G>C (p.Gly366Arg)	PRDM15 (G432R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218372	NM_001040424.3(PRDM15):c.1091A>C (p.Gln364Pro)	PRDM15 (Q364P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261345	NM_001040424.3(PRDM15):c.1063C>T (p.His355Tyr)	PRDM15 (H421Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218371	NM_001040424.3(PRDM15):c.1033C>T (p.Leu345Phe)	PRDM15 (L345F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218370	NM_001040424.3(PRDM15):c.1031C>T (p.Thr344Met)	PRDM15 (T344M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3250733	NM_001040424.3(PRDM15):c.1026C>T (p.Thr342=)	PRDM15	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3218368	NM_001040424.3(PRDM15):c.909T>G (p.Asp303Glu)	PRDM15 (D369E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218367	NM_001040424.3(PRDM15):c.905C>T (p.Pro302Leu)	PRDM15 (P302L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549526	NM_001040424.3(PRDM15):c.895G>A (p.Glu299Lys)	PRDM15 (E365K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652688	NM_001040424.3(PRDM15):c.894C>T (p.Thr298=)	PRDM15	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3309770	NM_001040424.3(PRDM15):c.862G>A (p.Glu288Lys)	PRDM15 (E288K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652689	NM_001040424.3(PRDM15):c.850G>A (p.Val284Met)	PRDM15 (V284M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2403341	NM_001040424.3(PRDM15):c.845T>C (p.Val282Ala)	PRDM15 (V348A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309759	NM_001040424.3(PRDM15):c.842T>C (p.Leu281Pro)	PRDM15 (L347P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592692	NM_001040424.3(PRDM15):c.800G>A (p.Arg267Gln)	PRDM15 (R267Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363959	NM_001040424.3(PRDM15):c.692A>G (p.Gln231Arg)	PRDM15 (Q297R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536768	NM_001040424.3(PRDM15):c.691C>G (p.Gln231Glu)	PRDM15 (Q231E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623886	NM_001040424.3(PRDM15):c.638A>G (p.Asn213Ser)	PRDM15 (N213S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531866	NM_001040424.3(PRDM15):c.588G>T (p.Gln196His)	PRDM15 (Q196H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218366	NM_001040424.3(PRDM15):c.569T>G (p.Val190Gly)	PRDM15 (V256G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532500	NM_001040424.3(PRDM15):c.541G>A (p.Ala181Thr)	PRDM15 (A181T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2570456	NM_001040424.3(PRDM15):c.274T>C (p.Phe92Leu)	PRDM15 (F158L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486175	NM_001040424.3(PRDM15):c.212A>G (p.Lys71Arg)	PRDM15 (K137R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220224	NM_001040424.3(PRDM15):c.131+549T>A	PRDM15 (V106E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307184	NM_001040424.3(PRDM15):c.131+524A>C	PRDM15 (T98P)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2334541	NM_001040424.3(PRDM15):c.131+502G>T	PRDM15 (Q90H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218364	NM_001040424.3(PRDM15):c.131+485C>T	PRDM15 (R85W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309758	NM_001040424.3(PRDM15):c.131+459A>G	PRDM15 (E76G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309763	NM_001040424.3(PRDM15):c.131+378G>T	PRDM15 (S49I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652692	NM_001040424.3(PRDM15):c.18C>T (p.Ser6=)	PRDM15	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2370650	NM_001040424.3(PRDM15):c.4G>A (p.Ala2Thr)	PRDM15 (A2T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456927	NM_001040424.3(PRDM15):c.-9-1192C>T	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2326542	NM_001040424.3(PRDM15):c.-9-1286G>A	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2652693	NM_001040424.3(PRDM15):c.-9-1296G>A	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2327373	NM_001040424.3(PRDM15):c.-9-1307G>T	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3309757	NM_001040424.3(PRDM15):c.-9-1331T>C	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3218394	NM_001040424.3(PRDM15):c.-9-1554A>C	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3218393	NM_001040424.3(PRDM15):c.-9-1605A>G	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2457161	NM_001040424.3(PRDM15):c.-9-1605A>T	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2363888	NM_001040424.3(PRDM15):c.-9-1609G>A	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2521645	NM_001040424.3(PRDM15):c.-9-1615G>A	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2375409	NM_001040424.3(PRDM15):c.-9-1627G>A	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2509296	NM_001040424.3(PRDM15):c.-9-6948G>A	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3218390	NM_001040424.3(PRDM15):c.-9-7003C>A	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2366491	NM_001040424.3(PRDM15):c.-10+7755C>T	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2408900	NM_001040424.3(PRDM15):c.-10+7737G>A	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3218385	NM_001040424.3(PRDM15):c.-10+7671G>T	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2608514	NM_001040424.3(PRDM15):c.-10+532G>C	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2491567	NM_001040424.3(PRDM15):c.-10+512C>G	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2591842	NM_001040424.3(PRDM15):c.-10+475C>T	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2475940	NM_001040424.3(PRDM15):c.-10+463G>T	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2397102	NM_001040424.3(PRDM15):c.-10+238C>G	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2536439	NM_001040424.3(PRDM15):c.-10+232C>T	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2534491	NM_001040424.3(PRDM15):c.-10+199T>G	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2611646	NM_001040424.3(PRDM15):c.-10+151C>T	PRDM15	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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