Related gene-specific medical variations for Gene (Select 414152) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3023845	NM_022124.6(CDH23):c.3370-20C>G	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3020058	NM_022124.6(CDH23):c.3615C>T (p.Ala1205=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3015023	NM_022124.6(CDH23):c.4207-14G>C	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3011643	NM_022124.6(CDH23):c.3580-17T>C	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3011480	NM_022124.6(CDH23):c.3580-6C>G	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3008596	NM_022124.6(CDH23):c.4207-12C>A	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3004381	NM_022124.6(CDH23):c.4020C>A (p.Ile1340=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2996152	NM_022124.6(CDH23):c.3282T>C (p.Asp1094=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2990752	NM_022124.6(CDH23):c.4207-10C>G	CDH23, C10orf105	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2986757	NM_022124.6(CDH23):c.4207-20G>A	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2971580	NM_022124.6(CDH23):c.3468T>C (p.Asn1156=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2914392	NM_022124.6(CDH23):c.3370-18T>C	CDH23, C10orf105	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2912294	NM_022124.6(CDH23):c.3580-4A>G	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2910378	NM_022124.6(CDH23):c.3716-4A>C	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2901566	NM_022124.6(CDH23):c.3370-20C>T	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2897772	NM_022124.6(CDH23):c.3430+19G>T	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2897417	NM_022124.6(CDH23):c.3474C>T (p.Leu1158=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2879385	NM_022124.6(CDH23):c.4209+1G>A	C10orf105, CDH23	Single nucleotide variant (splice donor variant +1 more)	not provided	GLikely pathogenic
Select item 2878287	NM_022124.6(CDH23):c.4173A>G (p.Ala1391=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2877406	NM_022124.6(CDH23):c.4206+12C>G	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2870503	NM_022124.6(CDH23):c.3539C>G (p.Ala1180Gly)	C10orf105, CDH23 (A1180G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2855522	NM_022124.6(CDH23):c.3897C>T (p.Val1299=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2855112	NM_022124.6(CDH23):c.4101C>T (p.Ile1367=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2851838	NM_022124.6(CDH23):c.3413G>A (p.Trp1138Ter)	C10orf105, CDH23 (W1138*)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 2849919	NM_022124.6(CDH23):c.4194G>T (p.Val1398=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2849070	NM_022124.6(CDH23):c.3579+19T>C	LOC126860953, C10orf105 +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2846529	NM_022124.6(CDH23):c.3561C>T (p.Pro1187=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2837781	NM_022124.6(CDH23):c.3855C>T (p.Ala1285=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2837736	NM_022124.6(CDH23):c.4104+17A>G	C10orf105, CDH23 (Q1374R)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2836626	NM_022124.6(CDH23):c.3243A>C (p.Arg1081=)	C10orf105, CDH23	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2834492	NM_022124.6(CDH23):c.3950dup (p.Tyr1318fs)	C10orf105, CDH23 (Y1318fs)	Duplication (frameshift variant +1 more)	not provided	GPathogenic
Select item 2833404	NM_001164375.3(C10orf105):c.*3104G>C	C10orf105, CDH23	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2831269	NM_022124.6(CDH23):c.4164A>G (p.Thr1388=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2828404	NM_022124.6(CDH23):c.3345C>T (p.Ile1115=)	C10orf105, CDH23	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2824440	NM_022124.6(CDH23):c.3579+20G>C	C10orf105, CDH23 +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2819985	NM_022124.6(CDH23):c.3321T>A (p.Tyr1107Ter)	C10orf105, CDH23 (Y1107*)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GPathogenic
Select item 2812773	NM_022124.6(CDH23):c.3431-15T>C	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2804191	NM_022124.6(CDH23):c.4206+14_4206+40del	C10orf105, CDH23	Deletion (intron variant)	not provided	GLikely benign
Select item 2800478	NM_022124.6(CDH23):c.3431-18G>T	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2793828	NM_022124.6(CDH23):c.3370-9C>T	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2787871	NM_022124.6(CDH23):c.3715+10G>T	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2779192	NM_001164375.3(C10orf105):c.*3291A>T	C10orf105, CDH23	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2779005	NM_022124.6(CDH23):c.3716-10C>G	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2772161	NM_022124.6(CDH23):c.3462C>A (p.Val1154=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2771922	NM_022124.6(CDH23):c.3828G>A (p.Lys1276=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2768269	NM_022124.6(CDH23):c.3481C>A (p.Arg1161=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2763587	NM_022124.6(CDH23):c.3541_3559del (p.Tyr1181fs)	C10orf105, CDH23 (Y1181fs)	Deletion (frameshift variant +1 more)	not provided	GPathogenic
Select item 2757273	NM_022124.6(CDH23):c.3431-19G>T	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2752737	NM_022124.6(CDH23):c.3801C>G (p.Thr1267=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2750893	NM_022124.6(CDH23):c.3222C>T (p.Asp1074=)	C10orf105, CDH23	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2740876	NM_022124.6(CDH23):c.3715+16G>A	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2740355	NM_022124.6(CDH23):c.3430+9G>A	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2735193	NM_022124.6(CDH23):c.3431-20G>T	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2726935	NM_022124.6(CDH23):c.3430+20G>T	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2724012	NM_022124.6(CDH23):c.3715+1G>A	C10orf105, CDH23	Single nucleotide variant (splice donor variant +1 more)	not provided	GLikely pathogenic
Select item 2711627	NM_022124.6(CDH23):c.3430+2T>C	C10orf105, CDH23	Single nucleotide variant (splice donor variant +1 more)	not provided	GLikely pathogenic
Select item 2706451	NM_022124.6(CDH23):c.4104+17A>C	C10orf105, CDH23 (Q1374P)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2706416	NM_022124.6(CDH23):c.3888C>T (p.Phe1296=)	CDH23, C10orf105	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2704478	NM_022124.6(CDH23):c.3579+13G>T	C10orf105, CDH23 +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2703179	NM_022124.6(CDH23):c.3834C>T (p.Ser1278=)	CDH23, C10orf105	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2699677	NM_022124.6(CDH23):c.3822G>A (p.Glu1274=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2697223	NM_022124.6(CDH23):c.3715+17G>A	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2680515	NM_022124.6(CDH23):c.3397G>T (p.Glu1133Ter)	C10orf105, CDH23 (E1133*)	Single nucleotide variant (nonsense +1 more)	Pituitary adenoma 5, multiple types	GLikely pathogenic
Select item 2680510	NM_022124.6(CDH23):c.3634C>T (p.Gln1212Ter)	C10orf105, CDH23 (Q1212*)	Single nucleotide variant (nonsense +1 more)	Pituitary adenoma 5, multiple types	GLikely pathogenic
Select item 2680507	NM_022124.6(CDH23):c.3769G>T (p.Glu1257Ter)	C10orf105, CDH23 (E1257*)	Single nucleotide variant (nonsense +1 more)	Pituitary adenoma 5, multiple types +1 more	GPathogenic/Likely pathogenic
Select item 2680505	NM_022124.6(CDH23):c.3720_3733del (p.Asp1240fs)	C10orf105, CDH23 (D1240fs)	Deletion (frameshift variant +1 more)	Pituitary adenoma 5, multiple types	GLikely pathogenic
Select item 2680500	NM_022124.6(CDH23):c.4207-2A>G	C10orf105, CDH23	Single nucleotide variant (splice acceptor variant +1 more)	Pituitary adenoma 5, multiple types +1 more	GLikely pathogenic
Select item 2680498	NM_022124.6(CDH23):c.4101_4104+3del	C10orf105, CDH23 (T1368fs)	Deletion (frameshift variant +2 more)	Pituitary adenoma 5, multiple types	GLikely pathogenic
Select item 2680476	NM_022124.6(CDH23):c.3486dup (p.Pro1163fs)	C10orf105, CDH23 (P1163fs)	Duplication (frameshift variant +1 more)	Pituitary adenoma 5, multiple types	GLikely pathogenic
Select item 2680458	NM_022124.6(CDH23):c.3591C>A (p.Tyr1197Ter)	C10orf105, CDH23 (Y1197*)	Single nucleotide variant (nonsense +1 more)	Pituitary adenoma 5, multiple types	GLikely pathogenic
Select item 2680451	NM_022124.6(CDH23):c.3292_3295dup (p.Arg1099fs)	C10orf105, CDH23 (R1099fs)	Duplication (3 prime UTR variant +1 more)	Pituitary adenoma 5, multiple types	GLikely pathogenic
Select item 2680449	NM_022124.6(CDH23):c.4195G>A (p.Asp1399Asn)	C10orf105, CDH23 (D1399N)	Single nucleotide variant (missense variant +1 more)	Pituitary adenoma 5, multiple types	GUncertain significance
Select item 2640572	NM_001164375.3(C10orf105):c.78C>T (p.Pro26=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2640571	NM_001164375.3(C10orf105):c.*490C>T	C10orf105, CDH23	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2610546	NM_022124.6(CDH23):c.3796A>G (p.Ile1266Val)	C10orf105, CDH23 (I1266V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2575872	NM_022124.6(CDH23):c.4051_4053delinsGAT (p.Asn1351Asp)	C10orf105, CDH23 (N1351D)	Indel (missense variant +1 more)	not provided	GUncertain significance
Select item 2542587	NM_022124.6(CDH23):c.3597G>T (p.Glu1199Asp)	C10orf105, CDH23 (E1199D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2538657	NM_022124.6(CDH23):c.3950C>T (p.Ser1317Leu)	C10orf105, CDH23 (S1317L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2506668	NM_022124.6(CDH23):c.3607G>A (p.Asp1203Asn)	C10orf105, CDH23 (D1203N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2467636	NM_022124.6(CDH23):c.3419G>A (p.Arg1140His)	CDH23, C10orf105 (R1140H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2439864	NM_022124.6(CDH23):c.3484G>A (p.Gly1162Arg)	C10orf105, CDH23 (G1162R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2419759	NM_022124.6(CDH23):c.3838A>C (p.Met1280Leu)	C10orf105, CDH23 (M1280L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2416921	NM_022124.6(CDH23):c.3580-19C>T	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2312594	NM_022124.6(CDH23):c.4109T>C (p.Val1370Ala)	C10orf105, CDH23 (V1370A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2266784	NM_022124.6(CDH23):c.3979G>T (p.Ala1327Ser)	C10orf105, CDH23 (A1327S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2226696	NM_001164375.3(C10orf105):c.170C>T (p.Thr57Met)	C10orf105, CDH23 (T57M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2202669	NM_022124.6(CDH23):c.4104+14G>A	C10orf105, CDH23 (G1373E)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2201960	NM_022124.6(CDH23):c.3580-20C>G	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2192003	NM_022124.6(CDH23):c.4018A>G (p.Ile1340Val)	CDH23, C10orf105 (I1340V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2190987	NM_022124.6(CDH23):c.3740G>A (p.Arg1247His)	C10orf105, CDH23 (R1247H)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2188393	NM_022124.6(CDH23):c.3226G>A (p.Gly1076Ser)	C10orf105, CDH23 (G1076S)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2177910	NM_022124.6(CDH23):c.4135C>T (p.Arg1379Cys)	C10orf105, CDH23 (R1379C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2175457	NM_022124.6(CDH23):c.3633G>T (p.Gln1211His)	C10orf105, CDH23 (Q1211H)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2170575	NM_022124.6(CDH23):c.3643C>A (p.Arg1215Ser)	CDH23, C10orf105 (R1215S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2167747	NM_022124.6(CDH23):c.3353G>T (p.Gly1118Val)	C10orf105, CDH23 (G1118V)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2166723	NM_022124.6(CDH23):c.4072G>A (p.Ala1358Thr)	C10orf105, CDH23 (A1358T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2166085	NM_022124.6(CDH23):c.3597G>A (p.Glu1199=)	C10orf105, CDH23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2163535	NM_022124.6(CDH23):c.3471G>A (p.Gly1157=)	CDH23, C10orf105	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2162500	NM_022124.6(CDH23):c.3430+11C>T	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2156084	NM_022124.6(CDH23):c.4204G>A (p.Val1402Met)	C10orf105, CDH23 (V1402M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

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