DGAT1[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1085353	NM_012079.6(DGAT1):c.1464C>T (p.Ala488=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1363716	NM_012079.6(DGAT1):c.1462G>A (p.Ala488Thr)	DGAT1 (A488T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 504005	NM_012079.6(DGAT1):c.1462del (p.Ala488fs)	DGAT1 (A488fs)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 1400812	NM_012079.6(DGAT1):c.1459G>A (p.Glu487Lys)	DGAT1 (E487K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1662297	NM_012079.6(DGAT1):c.1455G>T (p.Ala485=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1569835	NM_012079.6(DGAT1):c.1455G>A (p.Ala485=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 738939	NM_012079.6(DGAT1):c.1454C>T (p.Ala485Val)	DGAT1 (A485V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1422316	NM_012079.6(DGAT1):c.1450_1452del (p.Pro484del)	DGAT1 (P484del)	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 1905411	NM_012079.6(DGAT1):c.1449C>A (p.Ala483=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2184163	NM_012079.6(DGAT1):c.1443T>C (p.Tyr481=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1674523	NM_012079.6(DGAT1):c.1431C>T (p.Tyr477=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2316697	NM_012079.6(DGAT1):c.1427A>C (p.Tyr476Ser)	DGAT1 (Y476S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2092479	NM_012079.6(DGAT1):c.1425C>T (p.Asp475=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1167980	NM_012079.6(DGAT1):c.1422C>T (p.His474=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2978405	NM_012079.6(DGAT1):c.1419C>T (p.Val473=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1446023	NM_012079.6(DGAT1):c.1417G>A (p.Val473Ile)	DGAT1 (V473I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1950868	NM_012079.6(DGAT1):c.1416C>T (p.Tyr472=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1896603	NM_012079.6(DGAT1):c.1412T>C (p.Met471Thr)	DGAT1 (M471T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 722323	NM_012079.6(DGAT1):c.1407C>T (p.Val469=)	DGAT1	Single nucleotide variant (synonymous variant)	DGAT1-related disorder +1 more	GBenign/Likely benign
Select item 1523159	NM_012079.6(DGAT1):c.1405G>A (p.Val469Ile)	DGAT1 (V469I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1627760	NM_012079.6(DGAT1):c.1404C>T (p.Ala468=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 792119	NM_012079.6(DGAT1):c.1401A>T (p.Ile467=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1554867	NM_012079.6(DGAT1):c.1389C>T (p.Ile463=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2881266	NM_012079.6(DGAT1):c.1386C>T (p.Ile462=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2190282	NM_012079.6(DGAT1):c.1383C>T (p.Leu461=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3007957	NM_012079.6(DGAT1):c.1380G>A (p.Ser460=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2795495	NM_012079.6(DGAT1):c.1380G>T (p.Ser460=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1053416	NM_012079.6(DGAT1):c.1374G>A (p.Trp458Ter)	DGAT1 (W458*)	Single nucleotide variant (nonsense)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1961898	NM_012079.6(DGAT1):c.1373G>C (p.Trp458Ser)	DGAT1 (W458S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2192197	NM_012079.6(DGAT1):c.1368T>C (p.Ala456=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1922531	NM_012079.6(DGAT1):c.1362C>T (p.Asn454=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2111019	NM_012079.6(DGAT1):c.1348G>A (p.Gly450Ser)	DGAT1 (G450S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2015420	NM_012079.6(DGAT1):c.1346A>G (p.Gln449Arg)	DGAT1 (Q449R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2040791	NM_012079.6(DGAT1):c.1344C>T (p.Phe448=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1473571	NM_012079.6(DGAT1):c.1337_1338delinsAT (p.Arg446His)	DGAT1 (R446H)	Indel (missense variant)	not provided	GUncertain significance
Select item 2077745	NM_012079.6(DGAT1):c.1337G>A (p.Arg446His)	DGAT1 (R446H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2878442	NM_012079.6(DGAT1):c.1336del (p.Arg446fs)	DGAT1 (R446fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 1462841	NM_012079.6(DGAT1):c.1336C>T (p.Arg446Cys)	DGAT1 (R446C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1169249	NM_012079.6(DGAT1):c.1335C>T (p.Gly445=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1929232	NM_012079.6(DGAT1):c.1330G>A (p.Val444Met)	DGAT1 (V444M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1120466	NM_012079.6(DGAT1):c.1329C>T (p.Phe443=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1541823	NM_012079.6(DGAT1):c.1317A>G (p.Pro439=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2883483	NM_012079.6(DGAT1):c.1314C>T (p.Ile438=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1489526	NM_012079.6(DGAT1):c.1312-4del	DGAT1	Deletion (intron variant)	not provided	GLikely benign
Select item 1917516	NM_012079.6(DGAT1):c.1312-5C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3004980	NM_012079.6(DGAT1):c.1312-12C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2085357	NM_012079.6(DGAT1):c.1312-13C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2807179	NM_012079.6(DGAT1):c.1312-14C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2733314	NM_012079.6(DGAT1):c.1312-15C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1633893	NM_012079.6(DGAT1):c.1312-16G>A	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2831878	NM_012079.6(DGAT1):c.1311+13_1311+48del	DGAT1	Deletion (intron variant)	not provided	GLikely benign
Select item 2785846	NM_012079.6(DGAT1):c.1311+20C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2820722	NM_012079.6(DGAT1):c.1311+16G>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2793647	NM_012079.6(DGAT1):c.1311+16G>A	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1654300	NM_012079.6(DGAT1):c.1311+15C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2966571	NM_012079.6(DGAT1):c.1311+11C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2796772	NM_012079.6(DGAT1):c.1311+11C>A	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2789255	NM_012079.6(DGAT1):c.1311+10C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2831879	NM_012079.6(DGAT1):c.1311+9C>A	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1148020	NM_012079.6(DGAT1):c.1311+9C>T	DGAT1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1923379	NM_012079.6(DGAT1):c.1311+5G>A	DGAT1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1503319	NM_012079.6(DGAT1):c.1311+4A>G	DGAT1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1960248	NM_012079.6(DGAT1):c.1311+2T>C	DGAT1	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 489286	NM_012079.6(DGAT1):c.1311+1G>A	DGAT1	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 684436	NM_012079.6(DGAT1):c.1310A>G (p.Gln437Arg)	DGAT1 (Q437R)	Single nucleotide variant (missense variant)	Congenital diarrhea 7 with exudative enteropathy	GLikely pathogenic
Select item 1946397	NM_012079.6(DGAT1):c.1299C>T (p.Gly433=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1502536	NM_012079.6(DGAT1):c.1296G>A (p.Thr432=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2066108	NM_012079.6(DGAT1):c.1295C>T (p.Thr432Met)	DGAT1 (T432M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2719231	NM_012079.6(DGAT1):c.1290G>A (p.Ala430=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1352679	NM_012079.6(DGAT1):c.1270C>T (p.Arg424Ter)	DGAT1 (R424*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 3020192	NM_012079.6(DGAT1):c.1267C>T (p.Leu423=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3010332	NM_012079.6(DGAT1):c.1263C>T (p.Val421=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1626169	NM_012079.6(DGAT1):c.1260C>T (p.Ser420=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 391164	NM_012079.6(DGAT1):c.1260C>G (p.Ser420Arg)	DGAT1 (S420R)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2732274	NM_012079.6(DGAT1):c.1257G>C (p.Val419=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2036820	NM_012079.6(DGAT1):c.1254G>C (p.Leu418=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2702500	NM_012079.6(DGAT1):c.1251C>T (p.Tyr417=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2202070	NM_012079.6(DGAT1):c.1249-4T>C	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2764798	NM_012079.6(DGAT1):c.1249-9C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2851898	NM_012079.6(DGAT1):c.1249-10C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2835940	NM_012079.6(DGAT1):c.1249-11T>C	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2091359	NM_012079.6(DGAT1):c.1249-12C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2977268	NM_012079.6(DGAT1):c.1249-13C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3021275	NM_012079.6(DGAT1):c.1249-14C>G	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2983985	NM_012079.6(DGAT1):c.1249-15T>C	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2778060	NM_012079.6(DGAT1):c.1249-16C>G	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2842989	NM_012079.6(DGAT1):c.1249-17T>C	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1635249	NM_012079.6(DGAT1):c.1249-19T>C	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2030249	NM_012079.6(DGAT1):c.1248+17dup	DGAT1	Duplication (intron variant)	not provided	GBenign
Select item 2797078	NM_012079.6(DGAT1):c.1248+17G>A	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2706841	NM_012079.6(DGAT1):c.1248+15G>C	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2965514	NM_012079.6(DGAT1):c.1248+8C>T	DGAT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1978424	NM_012079.6(DGAT1):c.1248+4A>G	DGAT1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2501788	NM_012079.6(DGAT1):c.1246G>A (p.Glu416Lys)	DGAT1 (E416K)	Single nucleotide variant (missense variant)	Congenital diarrhea 7 with exudative enteropathy	GUncertain significance
Select item 1577748	NM_012079.6(DGAT1):c.1245C>T (p.His415=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1392882	NM_012079.6(DGAT1):c.1243C>T (p.His415Tyr)	DGAT1 (H415Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3005153	NM_012079.6(DGAT1):c.1239C>T (p.Phe413=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1477671	NM_012079.6(DGAT1):c.1233G>A (p.Ser411=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3002480	NM_012079.6(DGAT1):c.1227G>A (p.Leu409=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1943341	NM_012079.6(DGAT1):c.1224C>T (p.Phe408=)	DGAT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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