"GeneDx"[submitter] AND "DNAH6"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 669574	NM_003849.3(SUCLG1):c.-364T>C	DNAH6, SUCLG1	Single nucleotide variant (genic upstream transcript variant)	not provided	GBenign
Select item 673189	NM_003849.3(SUCLG1):c.-536A>C	DNAH6, LOC129934179 +1 more	Single nucleotide variant (genic upstream transcript variant)	not provided	GLikely benign
Select item 1265934	NM_001370.2(DNAH6):c.226-59A>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281178	NM_001370.2(DNAH6):c.400-21dup	DNAH6	Duplication (intron variant)	not provided	GBenign
Select item 1271750	NM_001370.2(DNAH6):c.400-22_400-21dup	DNAH6	Duplication (intron variant)	not provided	GBenign
Select item 402731	NM_001370.2(DNAH6):c.421G>A (p.Val141Met)	DNAH6 (V141M)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 3343264	NM_001370.2(DNAH6):c.594del (p.Gly200fs)	DNAH6 (G200fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 1261421	NM_001370.2(DNAH6):c.662+51T>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221478	NM_001370.2(DNAH6):c.662+160C>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234299	NM_001370.2(DNAH6):c.663-220T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 402732	NM_001370.2(DNAH6):c.786G>A (p.Leu262=)	DNAH6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 402733	NM_001370.2(DNAH6):c.873C>T (p.Ser291=)	DNAH6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1283783	NM_001370.2(DNAH6):c.1186+99A>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265733	NM_001370.2(DNAH6):c.1186+157G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282417	NM_001370.2(DNAH6):c.1316+132A>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250916	NM_001370.2(DNAH6):c.1485+166T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267159	NM_001370.2(DNAH6):c.1603-143G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 402734	NM_001370.2(DNAH6):c.1818C>A (p.Ala606=)	DNAH6	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 1294627	NM_001370.2(DNAH6):c.1924+187T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221610	NM_001370.2(DNAH6):c.2076+16A>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234602	NM_001370.2(DNAH6):c.2077-98G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281707	NM_001370.2(DNAH6):c.2229+139C>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258402	NM_001370.2(DNAH6):c.2481+29A>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1246505	NM_001370.2(DNAH6):c.2481+194dup	DNAH6	Duplication (intron variant)	not provided	GBenign
Select item 1279538	NM_001370.2(DNAH6):c.2482-202G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 402735	NM_001370.2(DNAH6):c.2547A>G (p.Gln849=)	DNAH6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1264385	NM_001370.2(DNAH6):c.2610+52G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266940	NM_001370.2(DNAH6):c.2610+100G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286393	NM_001370.2(DNAH6):c.2610+110G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280338	NM_001370.2(DNAH6):c.2611-153del	DNAH6	Deletion (intron variant)	not provided	GBenign
Select item 1264389	NM_001370.2(DNAH6):c.2611-107A>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276453	NM_001370.2(DNAH6):c.2724+198_2724+199insA	DNAH6	Insertion (intron variant)	not provided	GBenign
Select item 1271873	NM_001370.2(DNAH6):c.2725-221G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276950	NM_001370.2(DNAH6):c.2725-144T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257672	NM_001370.2(DNAH6):c.2725-55C>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274721	NM_001370.2(DNAH6):c.2869-198T>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229722	NM_001370.2(DNAH6):c.2869-187C>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262510	NM_001370.2(DNAH6):c.3081+92G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294644	NM_001370.2(DNAH6):c.3082-130del	DNAH6	Deletion (intron variant)	not provided	GBenign
Select item 1279364	NM_001370.2(DNAH6):c.3174+109T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228677	NM_001370.2(DNAH6):c.3175-216G>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280365	NM_001370.2(DNAH6):c.3175-37T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280020	NM_001370.2(DNAH6):c.3294+18T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256958	NM_001370.2(DNAH6):c.3294+156C>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283795	NM_001370.2(DNAH6):c.3294+177T>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179795	NM_001370.2(DNAH6):c.3294+185T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248631	NM_001370.2(DNAH6):c.3573-133C>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266361	NM_001370.2(DNAH6):c.3573-126A>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251710	NM_001370.2(DNAH6):c.3694A>G (p.Met1232Val)	DNAH6 (M1232V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1270327	NM_001370.2(DNAH6):c.3992G>A (p.Arg1331His)	DNAH6 (R1331H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1270255	NM_001370.2(DNAH6):c.4072-16T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279680	NM_001370.2(DNAH6):c.4353+19G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248423	NM_001370.2(DNAH6):c.4354-71T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 402736	NM_001370.2(DNAH6):c.4354-15C>T	DNAH6	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1236543	NM_001370.2(DNAH6):c.4515+41T>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268669	NM_001370.2(DNAH6):c.4516-209A>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 402737	NM_001370.2(DNAH6):c.4611C>T (p.Ile1537=)	DNAH6	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 1241750	NM_001370.2(DNAH6):c.4653+187C>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242049	NM_001370.2(DNAH6):c.4654-179C>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238852	NM_001370.2(DNAH6):c.4654-128C>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290832	NM_001370.2(DNAH6):c.4654-71C>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236303	NM_001370.2(DNAH6):c.4970+180G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234150	NM_001370.2(DNAH6):c.4970+219C>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294626	NM_001370.2(DNAH6):c.4971-163A>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 402738	NM_001370.2(DNAH6):c.5081G>C (p.Gly1694Ala)	DNAH6 (G1694A)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1223056	NM_001370.2(DNAH6):c.5331G>A (p.Gly1777=)	DNAH6	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1269923	NM_001370.2(DNAH6):c.5757+196T>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236942	NM_001370.2(DNAH6):c.5758-87G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232429	NM_001370.2(DNAH6):c.5940+17T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 775740	NM_001370.2(DNAH6):c.6090C>A (p.Pro2030=)	DNAH6	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1260974	NM_001370.2(DNAH6):c.6300G>A (p.Val2100=)	DNAH6	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1255160	NM_001370.2(DNAH6):c.6307-91T>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 402739	NM_001370.2(DNAH6):c.6356A>G (p.Tyr2119Cys)	DNAH6 (Y2119C)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 402740	NM_001370.2(DNAH6):c.6372A>G (p.Leu2124=)	DNAH6	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 1246507	NM_001370.2(DNAH6):c.6455-203T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288465	NM_001370.2(DNAH6):c.6455-91G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272996	NM_001370.2(DNAH6):c.6612+30G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279327	NM_001370.2(DNAH6):c.6612+153C>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280997	NM_001370.2(DNAH6):c.6803G>A (p.Ser2268Asn)	DNAH6 (S2268N)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1241815	NM_001370.2(DNAH6):c.6916+159C>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267646	NM_001370.2(DNAH6):c.7063+89T>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242024	NM_001370.2(DNAH6):c.7064-153C>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280418	NM_001370.2(DNAH6):c.7064-125A>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277453	NM_001370.2(DNAH6):c.7064-20T>G	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291870	NM_001370.2(DNAH6):c.7138-184dup	DNAH6	Duplication (intron variant)	not provided	GBenign
Select item 1275149	NM_001370.2(DNAH6):c.7138-94A>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1177941	NM_001370.2(DNAH6):c.7293-200G>C	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 402741	NM_001370.2(DNAH6):c.7353A>G (p.Thr2451=)	DNAH6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1245285	NM_001370.2(DNAH6):c.7525-80G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 402742	NM_001370.2(DNAH6):c.7649T>C (p.Val2550Ala)	DNAH6 (V2550A)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 1277186	NM_001370.2(DNAH6):c.7677+43G>A	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252924	NM_001370.2(DNAH6):c.7678-234C>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276730	NM_001370.2(DNAH6):c.7818+211del	DNAH6	Deletion (intron variant)	not provided	GBenign
Select item 1261832	NM_001370.2(DNAH6):c.7819-230C>T	DNAH6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274298	NM_001370.2(DNAH6):c.8229+142dup	DNAH6	Duplication (intron variant)	not provided	GBenign
Select item 1220646	NM_001370.2(DNAH6):c.8229+141_8229+142dup	DNAH6	Duplication (intron variant)	not provided	GBenign
Select item 1276536	NM_001370.2(DNAH6):c.8229+142del	DNAH6	Deletion (intron variant)	not provided	GBenign
Select item 2358631	NM_001370.2(DNAH6):c.8422G>A (p.Val2808Ile)	DNAH6 (V2808I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1267514	NM_001370.2(DNAH6):c.8576A>G (p.Lys2859Arg)	DNAH6 (K2859R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 402743	NM_001370.2(DNAH6):c.8692G>A (p.Val2898Ile)	DNAH6 (V2898I)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign

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