CORO6[gene] and "single gene"[properties] - ClinVar

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Items: 39

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2351335	NM_032854.4(CORO6):c.1412C>A (p.Thr471Lys)	CORO6 (T429K +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386369	NM_032854.4(CORO6):c.1408G>C (p.Gly470Arg)	CORO6 (G429R +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2229512	NM_032854.4(CORO6):c.1387A>G (p.Met463Val)	CORO6 (M388V +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3076410	NM_032854.4(CORO6):c.1348G>C (p.Val450Leu)	CORO6 (V450L +5 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 221307	NM_032854.4(CORO6):c.1348G>A (p.Val450Met)	CORO6 (V450M +5 more)	Single nucleotide variant (missense variant +1 more)	Breast ductal adenocarcinoma	GUncertain significance
Select item 2539459	NM_032854.4(CORO6):c.1346G>A (p.Arg449Gln)	CORO6 (R214Q +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2461599	NM_032854.4(CORO6):c.1262G>A (p.Arg421His)	CORO6 (R346H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222292	NM_032854.4(CORO6):c.1241G>A (p.Arg414His)	CORO6 (R373H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269033	NM_032854.4(CORO6):c.1186G>A (p.Val396Met)	CORO6 (V355M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598864	NM_032854.4(CORO6):c.1180G>C (p.Gly394Arg)	CORO6 (G319R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541434	NM_032854.4(CORO6):c.1178A>G (p.Asp393Gly)	CORO6 (D159G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226123	NM_032854.4(CORO6):c.1175G>T (p.Arg392Met)	CORO6 (R317M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2348627	NM_032854.4(CORO6):c.1106C>G (p.Pro369Arg)	CORO6 (P135R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3076408	NM_032854.4(CORO6):c.1100C>G (p.Pro367Arg)	CORO6 (P133R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528155	NM_032854.4(CORO6):c.1028A>G (p.Lys343Arg)	CORO6 (K303R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392254	NM_032854.4(CORO6):c.1024A>G (p.Arg342Gly)	CORO6 (R301G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489618	NM_032854.4(CORO6):c.901C>T (p.Pro301Ser)	CORO6 (P226S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269034	NM_032854.4(CORO6):c.895G>A (p.Glu299Lys)	CORO6 (E224K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3076417	NM_032854.4(CORO6):c.837C>G (p.Ser279Arg)	CORO6 (S279R +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2330624	NM_032854.4(CORO6):c.832T>G (p.Ser278Ala)	CORO6 (S238A +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2378680	NM_032854.4(CORO6):c.773T>C (p.Val258Ala)	CORO6 (V218A +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2411293	NM_032854.4(CORO6):c.751C>T (p.Pro251Ser)	CORO6 (P210S +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2299531	NM_032854.4(CORO6):c.722T>A (p.Met241Lys)	CORO6 (M200K +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 3076415	NM_032854.4(CORO6):c.671G>C (p.Arg224Pro)	CORO6 (R183P +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 3076414	NM_032854.4(CORO6):c.664C>G (p.Pro222Ala)	CORO6 (P181A +1 more)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 3076413	NM_032854.4(CORO6):c.632C>T (p.Ala211Val)	CORO6 (A170V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531573	NM_032854.4(CORO6):c.599G>T (p.Arg200Leu)	CORO6 (R159L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269035	NM_032854.4(CORO6):c.464T>A (p.Val155Glu)	CORO6 (V114E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308686	NM_032854.4(CORO6):c.409C>T (p.Leu137Phe)	CORO6 (L96F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379241	NM_032854.4(CORO6):c.377C>T (p.Thr126Ile)	CORO6 (T126I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399507	NM_032854.4(CORO6):c.353G>A (p.Arg118His)	CORO6 (R118H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320571	NM_032854.4(CORO6):c.347C>G (p.Pro116Arg)	CORO6 (P116R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3076412	NM_032854.4(CORO6):c.319A>C (p.Met107Leu)	CORO6 (M107L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2354221	NM_032854.4(CORO6):c.316A>T (p.Ile106Phe)	CORO6 (I106F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2257137	NM_032854.4(CORO6):c.203G>A (p.Gly68Glu)	CORO6 (G68E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2551831	NM_032854.4(CORO6):c.170G>T (p.Gly57Val)	CORO6 (G57V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3076411	NM_032854.4(CORO6):c.166G>A (p.Gly56Arg)	CORO6 (G56R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3076409	NM_032854.4(CORO6):c.124G>A (p.Val42Ile)	CORO6 (V42I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3076416	NM_032854.4(CORO6):c.7A>G (p.Arg3Gly)	CORO6 (R3G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 39