CDHR2[gene] and "single gene"[properties] - ClinVar

Search results

Items: 91

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2331204	NM_017675.6(CDHR2):c.71C>T (p.Pro24Leu)	CDHR2 (P24L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2497709	NM_017675.6(CDHR2):c.92C>T (p.Thr31Met)	CDHR2 (T31M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3141360	NM_017675.6(CDHR2):c.169C>T (p.Pro57Ser)	CDHR2 (P57S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351527	NM_017675.6(CDHR2):c.186G>T (p.Met62Ile)	CDHR2 (M62I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2592750	NM_017675.6(CDHR2):c.211G>A (p.Ala71Thr)	CDHR2 (A71T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2242048	NM_017675.6(CDHR2):c.241C>G (p.Leu81Val)	CDHR2 (L81V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656086	NM_017675.6(CDHR2):c.249C>T (p.Ser83=)	CDHR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2389543	NM_017675.6(CDHR2):c.289A>G (p.Ile97Val)	CDHR2 (I97V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656087	NM_017675.6(CDHR2):c.366C>T (p.Pro122=)	CDHR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2404181	NM_017675.6(CDHR2):c.367G>A (p.Val123Ile)	CDHR2 (V123I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141380	NM_017675.6(CDHR2):c.491A>T (p.Glu164Val)	CDHR2 (E164V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607513	NM_017675.6(CDHR2):c.664T>G (p.Ser222Ala)	CDHR2 (S222A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350395	NM_017675.6(CDHR2):c.740C>T (p.Ser247Leu)	CDHR2 (S247L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349382	NM_017675.6(CDHR2):c.785C>T (p.Thr262Met)	CDHR2 (T262M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324825	NM_017675.6(CDHR2):c.842C>T (p.Ser281Phe)	CDHR2 (S281F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508308	NM_017675.6(CDHR2):c.851C>A (p.Thr284Lys)	CDHR2 (T284K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141381	NM_017675.6(CDHR2):c.881A>T (p.Asp294Val)	CDHR2 (D294V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141382	NM_017675.6(CDHR2):c.914G>C (p.Arg305Pro)	CDHR2 (R305P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141356	NM_017675.6(CDHR2):c.1096G>A (p.Glu366Lys)	CDHR2 (E366K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141357	NM_017675.6(CDHR2):c.1126G>A (p.Val376Met)	CDHR2 (V376M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405824	NM_017675.6(CDHR2):c.1133A>T (p.Glu378Val)	CDHR2 (E378V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313876	NM_017675.6(CDHR2):c.1147C>G (p.Arg383Gly)	CDHR2 (R383G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656088	NM_017675.6(CDHR2):c.1188G>A (p.Pro396=)	CDHR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2321477	NM_017675.6(CDHR2):c.1196G>A (p.Gly399Asp)	CDHR2 (G399D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656089	NM_017675.6(CDHR2):c.1221G>A (p.Ser407=)	CDHR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2483915	NM_017675.6(CDHR2):c.1267G>A (p.Ala423Thr)	CDHR2 (A423T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355012	NM_017675.6(CDHR2):c.1285G>A (p.Val429Ile)	CDHR2 (V429I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141358	NM_017675.6(CDHR2):c.1297G>A (p.Val433Met)	CDHR2 (V433M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402821	NM_017675.6(CDHR2):c.1352T>C (p.Val451Ala)	CDHR2 (V451A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141359	NM_017675.6(CDHR2):c.1436C>T (p.Thr479Met)	CDHR2 (T479M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266438	NM_017675.6(CDHR2):c.1452G>T (p.Leu484Phe)	CDHR2 (L484F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304902	NM_017675.6(CDHR2):c.1456G>A (p.Val486Ile)	CDHR2 (V486I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2328932	NM_017675.6(CDHR2):c.1501G>A (p.Asp501Asn)	CDHR2 (D501N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2226388	NM_017675.6(CDHR2):c.1534G>A (p.Ala512Thr)	CDHR2 (A512T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527987	NM_017675.6(CDHR2):c.1557C>G (p.Ser519Arg)	CDHR2 (S519R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536939	NM_017675.6(CDHR2):c.1568G>A (p.Gly523Glu)	CDHR2 (G523E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300229	NM_017675.6(CDHR2):c.1612G>C (p.Val538Leu)	CDHR2 (V538L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401986	NM_017675.6(CDHR2):c.1616C>T (p.Thr539Met)	CDHR2 (T539M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337981	NM_017675.6(CDHR2):c.1901C>G (p.Ser634Cys)	CDHR2 (S634C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541280	NM_017675.6(CDHR2):c.1909C>A (p.Pro637Thr)	CDHR2 (P637T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141362	NM_017675.6(CDHR2):c.1966G>A (p.Ala656Thr)	CDHR2 (A656T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411689	NM_017675.6(CDHR2):c.1979G>A (p.Arg660His)	CDHR2 (R660H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656090	NM_017675.6(CDHR2):c.2014G>A (p.Glu672Lys)	CDHR2 (E672K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2656091	NM_017675.6(CDHR2):c.2066A>G (p.Asn689Ser)	CDHR2 (N689S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2588180	NM_017675.6(CDHR2):c.2161G>A (p.Ala721Thr)	CDHR2 (A721T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141363	NM_017675.6(CDHR2):c.2194T>G (p.Phe732Val)	CDHR2 (F732V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327271	NM_017675.6(CDHR2):c.2266G>A (p.Gly756Ser)	CDHR2 (G756S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405884	NM_017675.6(CDHR2):c.2276G>A (p.Arg759Gln)	CDHR2 (R759Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141364	NM_017675.6(CDHR2):c.2279T>C (p.Leu760Pro)	CDHR2 (L760P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141366	NM_017675.6(CDHR2):c.2305G>A (p.Glu769Lys)	CDHR2 (E769K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239756	NM_017675.6(CDHR2):c.2339C>G (p.Ala780Gly)	CDHR2 (A780G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515491	NM_017675.6(CDHR2):c.2359G>C (p.Gly787Arg)	CDHR2 (G787R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354194	NM_017675.6(CDHR2):c.2359G>T (p.Gly787Trp)	CDHR2 (G787W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359965	NM_017675.6(CDHR2):c.2362G>T (p.Gly788Cys)	CDHR2 (G788C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359668	NM_017675.6(CDHR2):c.2365G>A (p.Glu789Lys)	CDHR2 (E789K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656092	NM_017675.6(CDHR2):c.2385C>T (p.Cys795=)	CDHR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2286571	NM_017675.6(CDHR2):c.2410A>T (p.Asn804Tyr)	CDHR2 (N804Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141367	NM_017675.6(CDHR2):c.2449C>T (p.Arg817Cys)	CDHR2 (R817C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141368	NM_017675.6(CDHR2):c.2501C>T (p.Ser834Leu)	CDHR2 (S834L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616444	NM_017675.6(CDHR2):c.2552G>A (p.Cys851Tyr)	CDHR2 (C851Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362437	NM_017675.6(CDHR2):c.2630A>G (p.Asn877Ser)	CDHR2 (N877S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243990	NM_017675.6(CDHR2):c.2655G>T (p.Glu885Asp)	CDHR2 (E885D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210918	NM_017675.6(CDHR2):c.2672C>T (p.Thr891Met)	CDHR2 (T891M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656093	NM_017675.6(CDHR2):c.2703G>A (p.Thr901=)	CDHR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3141369	NM_017675.6(CDHR2):c.2761G>A (p.Val921Met)	CDHR2 (V921M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141370	NM_017675.6(CDHR2):c.2824G>A (p.Val942Met)	CDHR2 (V942M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141371	NM_017675.6(CDHR2):c.2914G>C (p.Asp972His)	CDHR2 (D972H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545512	NM_017675.6(CDHR2):c.2932G>C (p.Gly978Arg)	CDHR2 (G978R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411243	NM_017675.6(CDHR2):c.2986G>A (p.Asp996Asn)	CDHR2 (D996N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3141373	NM_017675.6(CDHR2):c.2989G>A (p.Val997Met)	CDHR2 (V997M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328333	NM_017675.6(CDHR2):c.2996C>T (p.Ala999Val)	CDHR2 (A999V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614806	NM_017675.6(CDHR2):c.3085G>A (p.Gly1029Ser)	CDHR2 (G1029S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245208	NM_017675.6(CDHR2):c.3149G>A (p.Arg1050Gln)	CDHR2 (R1050Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141374	NM_017675.6(CDHR2):c.3380T>C (p.Leu1127Pro)	CDHR2 (L1127P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335485	NM_017675.6(CDHR2):c.3415G>C (p.Gly1139Arg)	CDHR2 (G1139R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141375	NM_017675.6(CDHR2):c.3426G>C (p.Glu1142Asp)	CDHR2 (E1142D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344055	NM_017675.6(CDHR2):c.3473G>C (p.Gly1158Ala)	CDHR2 (G1158A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604308	NM_017675.6(CDHR2):c.3484G>A (p.Ala1162Thr)	CDHR2 (A1162T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348937	NM_017675.6(CDHR2):c.3523G>A (p.Val1175Met)	CDHR2 (V1175M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3141376	NM_017675.6(CDHR2):c.3532C>T (p.Arg1178Trp)	CDHR2 (R1178W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245258	NM_017675.6(CDHR2):c.3533G>A (p.Arg1178Gln)	CDHR2 (R1178Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256054	NM_017675.6(CDHR2):c.3545A>G (p.Asn1182Ser)	CDHR2 (N1182S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312931	NM_017675.6(CDHR2):c.3548G>T (p.Arg1183Leu)	CDHR2 (R1183L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375776	NM_017675.6(CDHR2):c.3553C>A (p.Leu1185Ile)	CDHR2 (L1185I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370523	NM_017675.6(CDHR2):c.3577G>A (p.Glu1193Lys)	CDHR2 (E1193K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495882	NM_017675.6(CDHR2):c.3722T>G (p.Leu1241Arg)	CDHR2 (L1241R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465005	NM_017675.6(CDHR2):c.3736G>A (p.Val1246Ile)	CDHR2 (V1246I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2618540	NM_017675.6(CDHR2):c.3795G>C (p.Glu1265Asp)	CDHR2 (E1265D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141378	NM_017675.6(CDHR2):c.3859C>T (p.Arg1287Trp)	CDHR2 (R1287W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141379	NM_017675.6(CDHR2):c.3916G>C (p.Asp1306His)	CDHR2 (D1306H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250021	NM_017675.6(CDHR2):c.3923C>T (p.Thr1308Met)	CDHR2 (T1308M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 91