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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2343230	NM_014675.5(CROCC):c.76G>A (p.Val26Ile)	CROCC (V26I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457397	NM_014675.5(CROCC):c.104C>T (p.Ala35Val)	CROCC (A35V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2516674	NM_014675.5(CROCC):c.124G>A (p.Ala42Thr)	CROCC (A42T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523026	NM_014675.5(CROCC):c.155G>A (p.Arg52Lys)	CROCC (R52K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077579	NM_014675.5(CROCC):c.169C>T (p.Arg57Cys)	CROCC (R57C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516241	NM_014675.5(CROCC):c.182A>G (p.Gln61Arg)	CROCC (Q61R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2465199	NM_014675.5(CROCC):c.189G>C (p.Glu63Asp)	CROCC (E63D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262910	NM_014675.5(CROCC):c.193C>A (p.Pro65Thr)	CROCC (P65T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237799	NM_014675.5(CROCC):c.208G>A (p.Ala70Thr)	CROCC (A70T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 767658	NM_014675.5(CROCC):c.213A>G (p.Thr71=)	CROCC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2262432	NM_014675.5(CROCC):c.220G>C (p.Ala74Pro)	CROCC (A74P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077593	NM_014675.5(CROCC):c.275G>A (p.Arg92His)	CROCC (R92H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280618	NM_014675.5(CROCC):c.338C>T (p.Ala113Val)	CROCC (A113V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077600	NM_014675.5(CROCC):c.356A>G (p.Glu119Gly)	CROCC (E119G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411723	NM_014675.5(CROCC):c.367C>T (p.Arg123Trp)	CROCC (R123W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366960	NM_014675.5(CROCC):c.399G>T (p.Glu133Asp)	CROCC (E133D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077610	NM_014675.5(CROCC):c.466C>T (p.Arg156Trp)	CROCC (R156W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456557	NM_014675.5(CROCC):c.502C>T (p.Arg168Trp)	CROCC (R168W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2638365	NM_014675.5(CROCC):c.538-4C>A	CROCC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2385796	NM_014675.5(CROCC):c.548A>G (p.Tyr183Cys)	CROCC (Y183C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2638366	NM_014675.5(CROCC):c.564G>A (p.Ser188=)	CROCC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3077616	NM_014675.5(CROCC):c.584T>G (p.Leu195Arg)	CROCC (L195R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2638367	NM_014675.5(CROCC):c.614G>A (p.Arg205Gln)	CROCC (R205Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 790475	NM_014675.5(CROCC):c.625A>G (p.Thr209Ala)	CROCC (T209A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3077617	NM_014675.5(CROCC):c.670G>A (p.Glu224Lys)	CROCC (E224K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309597	NM_014675.5(CROCC):c.697G>A (p.Ala233Thr)	CROCC (A233T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403665	NM_014675.5(CROCC):c.719G>A (p.Arg240Gln)	CROCC (R240Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251190	NM_014675.5(CROCC):c.743C>T (p.Ser248Leu)	CROCC (S248L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248692	NM_014675.5(CROCC):c.768C>G (p.Asp256Glu)	CROCC (D256E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239760	NM_014675.5(CROCC):c.772C>G (p.Arg258Gly)	CROCC (R258G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589477	NM_014675.5(CROCC):c.796C>T (p.Arg266Cys)	CROCC (R266C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 731787	NM_014675.5(CROCC):c.799T>A (p.Cys267Ser)	CROCC (C267S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2638368	NM_014675.5(CROCC):c.819C>G (p.His273Gln)	CROCC (H273Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2638369	NM_014675.5(CROCC):c.831G>A (p.Ala277=)	CROCC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2215921	NM_014675.5(CROCC):c.839G>A (p.Arg280His)	CROCC (R280H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546920	NM_014675.5(CROCC):c.841G>A (p.Glu281Lys)	CROCC (E281K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366238	NM_014675.5(CROCC):c.902G>A (p.Arg301Lys)	CROCC (R301K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1686401	NM_014675.5(CROCC):c.904C>G (p.Gln302Glu)	CROCC (Q302E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2235848	NM_014675.5(CROCC):c.922C>T (p.Arg308Trp)	CROCC (R308W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2638370	NM_014675.5(CROCC):c.1014G>A (p.Ala338=)	CROCC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2638371	NM_014675.5(CROCC):c.1032G>A (p.Thr344=)	CROCC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2386125	NM_014675.5(CROCC):c.1054C>T (p.Arg352Trp)	CROCC (R352W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286097	NM_014675.5(CROCC):c.1085T>C (p.Leu362Pro)	CROCC (L362P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3067232	NM_014675.5(CROCC):c.1113G>C (p.Leu371=)	CROCC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2638372	NM_014675.5(CROCC):c.1131C>T (p.Arg377=)	CROCC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3077574	NM_014675.5(CROCC):c.1165G>A (p.Asp389Asn)	CROCC (D389N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3025800	NM_014675.5(CROCC):c.1290+8G>T	CROCC	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3077575	NM_014675.5(CROCC):c.1363G>A (p.Asp455Asn)	CROCC (D455N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295106	NM_014675.5(CROCC):c.1378G>T (p.Val460Phe)	CROCC (V460F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477281	NM_014675.5(CROCC):c.1399G>A (p.Gly467Ser)	CROCC (G467S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077576	NM_014675.5(CROCC):c.1412G>C (p.Ser471Thr)	CROCC (S471T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280346	NM_014675.5(CROCC):c.1413C>G (p.Ser471Arg)	CROCC (S471R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222642	NM_014675.5(CROCC):c.1441A>T (p.Asn481Tyr)	CROCC (N481Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369585	NM_014675.5(CROCC):c.1444G>A (p.Gly482Ser)	CROCC (G482S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227595	NM_014675.5(CROCC):c.1454G>C (p.Arg485Pro)	CROCC (R485P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211707	NM_014675.5(CROCC):c.1456G>A (p.Gly486Arg)	CROCC (G486R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2672325	NM_014675.5(CROCC):c.1463C>T (p.Ser488Leu)	CROCC (S488L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2538342	NM_014675.5(CROCC):c.1484C>G (p.Pro495Arg)	CROCC (P495R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623063	NM_014675.5(CROCC):c.1486C>G (p.Pro496Ala)	CROCC (P496A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411843	NM_014675.5(CROCC):c.1504G>A (p.Gly502Ser)	CROCC (G502S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385316	NM_014675.5(CROCC):c.1507C>G (p.Arg503Gly)	CROCC (R503G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278652	NM_014675.5(CROCC):c.1519C>T (p.Pro507Ser)	CROCC (P507S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077578	NM_014675.5(CROCC):c.1571T>C (p.Ile524Thr)	CROCC (I524T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283927	NM_014675.5(CROCC):c.1577C>G (p.Ser526Cys)	CROCC (S526C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389019	NM_014675.5(CROCC):c.1643T>G (p.Leu548Arg)	CROCC (L548R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354329	NM_014675.5(CROCC):c.1714C>T (p.Arg572Cys)	CROCC (R572C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593005	NM_014675.5(CROCC):c.1720C>G (p.Arg574Gly)	CROCC (R574G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309664	NM_014675.5(CROCC):c.1723G>A (p.Asp575Asn)	CROCC (D575N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2638373	NM_014675.5(CROCC):c.1734C>T (p.Asp578=)	CROCC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2257248	NM_014675.5(CROCC):c.1734C>G (p.Asp578Glu)	CROCC (D578E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397866	NM_014675.5(CROCC):c.1735G>A (p.Gly579Ser)	CROCC (G579S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397867	NM_014675.5(CROCC):c.1738G>A (p.Ala580Thr)	CROCC (A580T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2564867	NM_014675.5(CROCC):c.1794C>A (p.Asn598Lys)	CROCC (N598K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2564482	NM_014675.5(CROCC):c.1826C>T (p.Ala609Val)	CROCC (A609V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077581	NM_014675.5(CROCC):c.1855G>T (p.Ala619Ser)	CROCC (A619S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396530	NM_014675.5(CROCC):c.1876C>T (p.Arg626Trp)	CROCC (R626W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225878	NM_014675.5(CROCC):c.1892C>T (p.Ala631Val)	CROCC (A631V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348783	NM_014675.5(CROCC):c.1910G>A (p.Arg637Gln)	CROCC (R637Q)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2638374	NM_014675.5(CROCC):c.1947C>T (p.Asp649=)	CROCC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2530482	NM_014675.5(CROCC):c.1978G>C (p.Glu660Gln)	CROCC (E660Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077582	NM_014675.5(CROCC):c.1997G>T (p.Arg666Ile)	CROCC (R666I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 774151	NM_014675.5(CROCC):c.2024G>A (p.Arg675His)	CROCC (R675H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3077584	NM_014675.5(CROCC):c.2053G>A (p.Val685Met)	CROCC (V685M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 772652	NM_014675.5(CROCC):c.2072G>A (p.Arg691His)	CROCC (R691H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2365702	NM_014675.5(CROCC):c.2104G>A (p.Glu702Lys)	CROCC (E702K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239758	NM_014675.5(CROCC):c.2126C>T (p.Ala709Val)	CROCC (A709V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261853	NM_014675.5(CROCC):c.2137G>A (p.Ala713Thr)	CROCC (A713T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077585	NM_014675.5(CROCC):c.2149C>T (p.Arg717Cys)	CROCC (R717C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509044	NM_014675.5(CROCC):c.2150G>A (p.Arg717His)	CROCC (R717H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481975	NM_014675.5(CROCC):c.2182A>G (p.Arg728Gly)	CROCC (R728G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345145	NM_014675.5(CROCC):c.2189A>G (p.Glu730Gly)	CROCC (E730G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2638375	NM_014675.5(CROCC):c.2304C>T (p.Ala768=)	CROCC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3077586	NM_014675.5(CROCC):c.2315G>A (p.Arg772Gln)	CROCC (R772Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272794	NM_014675.5(CROCC):c.2342C>T (p.Thr781Ile)	CROCC (T781I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362473	NM_014675.5(CROCC):c.2351G>A (p.Arg784Gln)	CROCC (R784Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077587	NM_014675.5(CROCC):c.2365C>T (p.Arg789Trp)	CROCC (R789W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466670	NM_014675.5(CROCC):c.2366G>A (p.Arg789Gln)	CROCC (R789Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326725	NM_014675.5(CROCC):c.2389C>G (p.Gln797Glu)	CROCC (Q797E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077588	NM_014675.5(CROCC):c.2401C>T (p.Arg801Trp)	CROCC (R801W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287913	NM_014675.5(CROCC):c.2441C>G (p.Ala814Gly)	CROCC (A814G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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