"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "AKT1"[g - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1009874	NM_001382430.1(AKT1):c.1440C>G (p.Ala480=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6	GUncertain significance
Select item 1549857	NM_001382430.1(AKT1):c.1437G>T (p.Thr479=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6	GLikely benign
Select item 1126278	NM_001382430.1(AKT1):c.1437G>A (p.Thr479=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 1006787	NM_001382430.1(AKT1):c.1436C>T (p.Thr479Met)	AKT1 (T479M)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 575013	NM_001382430.1(AKT1):c.1432G>A (p.Gly478Ser)	AKT1 (G478S)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 240110	NM_001382430.1(AKT1):c.1431C>T (p.Ser477=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 1772362	NM_001382430.1(AKT1):c.1425G>A (p.Ser475=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +2 more	GConflicting classifications of pathogenicity
Select item 1153354	NM_001382430.1(AKT1):c.1419C>G (p.Ser473=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 699745	NM_001382430.1(AKT1):c.1416C>T (p.Phe472=)	AKT1	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 2811135	NM_001382430.1(AKT1):c.1399C>T (p.Pro467Ser)	AKT1 (P467S)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 2123387	NM_001382430.1(AKT1):c.1397G>A (p.Arg466Lys)	AKT1 (R466K)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 1975172	NM_001382430.1(AKT1):c.1395C>G (p.Arg465=)	AKT1	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 220815	NM_001382430.1(AKT1):c.1394G>A (p.Arg465His)	AKT1 (R465H)	Single nucleotide variant (missense variant)	Cowden syndrome 6 +5 more	GConflicting classifications of pathogenicity
Select item 1018655	NM_001382430.1(AKT1):c.1393C>T (p.Arg465Cys)	AKT1 (R465C)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 584874	NM_001382430.1(AKT1):c.1390G>A (p.Glu464Lys)	AKT1 (E464K)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 240109	NM_001382430.1(AKT1):c.1389C>T (p.Ser463=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6	GBenign
Select item 1771429	NM_001382430.1(AKT1):c.1387A>G (p.Ser463Gly)	AKT1 (S463G)	Single nucleotide variant (missense variant)	Cowden syndrome 6 +1 more	GUncertain significance
Select item 1771408	NM_001382430.1(AKT1):c.1386C>T (p.Asp462=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 1570477	NM_001382430.1(AKT1):c.1383G>A (p.Val461=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6	GLikely benign
Select item 240108	NM_001382430.1(AKT1):c.1380T>C (p.Cys460=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 2039863	NM_001382430.1(AKT1):c.1373T>A (p.Met458Lys)	AKT1 (M458K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 133454	NM_001382430.1(AKT1):c.1373T>C (p.Met458Thr)	AKT1 (M458T)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 1040994	NM_001382430.1(AKT1):c.1372A>G (p.Met458Val)	AKT1 (M458V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1686412	NM_001382430.1(AKT1):c.1364-3C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6 +1 more	GConflicting classifications of pathogenicity
Select item 2178099	NM_001382430.1(AKT1):c.1364-9C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 2060517	NM_001382430.1(AKT1):c.1364-10A>C	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 696737	NM_001382430.1(AKT1):c.1364-10A>G	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 2087446	NM_001382430.1(AKT1):c.1364-11T>C	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1599653	NM_001382430.1(AKT1):c.1364-11del	AKT1	Deletion (intron variant)	Cowden syndrome 6	GBenign
Select item 1600702	NM_001382430.1(AKT1):c.1363+12C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GBenign
Select item 702764	NM_001382430.1(AKT1):c.1363+9C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 540891	NM_001382430.1(AKT1):c.1361A>G (p.Gln454Arg)	AKT1 (Q454R)	Single nucleotide variant (missense variant)	Cowden syndrome 6 +1 more	GUncertain significance
Select item 2725335	NM_001382430.1(AKT1):c.1357G>C (p.Asp453His)	AKT1 (D453H)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 2771149	NM_001382430.1(AKT1):c.1345A>T (p.Ile449Phe)	AKT1 (I449F)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 416467	NM_001382430.1(AKT1):c.1341C>A (p.Ile447=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6	GLikely benign
Select item 1362051	NM_001382430.1(AKT1):c.1338G>T (p.Met446Ile)	AKT1 (M446I)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 240107	NM_001382430.1(AKT1):c.1329G>A (p.Thr443=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 2188658	NM_001382430.1(AKT1):c.1323G>A (p.Glu441=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6	GLikely benign
Select item 473852	NM_001382430.1(AKT1):c.1320G>T (p.Glu440Asp)	AKT1 (E440D)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 2814661	NM_001382430.1(AKT1):c.1318G>A (p.Glu440Lys)	AKT1 (E440K)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 1769682	NM_001382430.1(AKT1):c.1311T>C (p.Tyr437=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 2736828	NM_001382430.1(AKT1):c.1305C>T (p.Thr435=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6	GLikely benign
Select item 540908	NM_001382430.1(AKT1):c.1293G>A (p.Ser431=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 1769135	NM_001382430.1(AKT1):c.1292C>T (p.Ser431Leu)	AKT1 (S431L)	Single nucleotide variant (missense variant)	Cowden syndrome 6 +1 more	GUncertain significance
Select item 540895	NM_001382430.1(AKT1):c.1290G>A (p.Thr430=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 853634	NM_001382430.1(AKT1):c.1289C>T (p.Thr430Met)	AKT1 (T430M)	Single nucleotide variant (missense variant)	Colorectal cancer +4 more	GUncertain significance
Select item 1768696	NM_001382430.1(AKT1):c.1284G>A (p.Gln428=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 1768078	NM_001382430.1(AKT1):c.1281C>T (p.Pro427=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 758409	NM_001382430.1(AKT1):c.1278G>A (p.Lys426=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6	GLikely benign
Select item 1016933	NM_001382430.1(AKT1):c.1277A>C (p.Lys426Thr)	AKT1 (K426T)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 1764453	NM_001382430.1(AKT1):c.1267C>T (p.Pro423Ser)	AKT1 (P423S)	Single nucleotide variant (missense variant)	Cowden syndrome 6 +1 more	GUncertain significance
Select item 569447	NM_001382430.1(AKT1):c.1261C>T (p.Leu421Phe)	AKT1 (L421F)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 3018963	NM_001382430.1(AKT1):c.1261-8C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1134032	NM_001382430.1(AKT1):c.1261-10A>C	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1624258	NM_001382430.1(AKT1):c.1261-18G>A	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1585233	NM_001382430.1(AKT1):c.1261-19C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1662392	NM_001382430.1(AKT1):c.1261-20C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 2896445	NM_001382430.1(AKT1):c.1260+19T>C	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1536764	NM_001382430.1(AKT1):c.1260+18A>G	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1603034	NM_001382430.1(AKT1):c.1260+16G>A	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1531541	NM_001382430.1(AKT1):c.1260+15C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1558345	NM_001382430.1(AKT1):c.1260+12C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GBenign
Select item 2108446	NM_001382430.1(AKT1):c.1260+7C>G	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 725843	NM_001382430.1(AKT1):c.1260+7C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 847554	NM_001382430.1(AKT1):c.1260+5G>A	AKT1	Single nucleotide variant (intron variant)	AKT1-related disorder +5 more	GUncertain significance
Select item 410906	NM_001382430.1(AKT1):c.1260+4C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GUncertain significance
Select item 1022066	NM_001382430.1(AKT1):c.1260+1G>C	AKT1	Single nucleotide variant (splice donor variant)	Cowden syndrome 6	GUncertain significance
Select item 221141	NM_001382430.1(AKT1):c.1251C>T (p.Tyr417=)	AKT1	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 1122647	NM_001382430.1(AKT1):c.1248G>A (p.Val416=)	AKT1	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 1538724	NM_001382430.1(AKT1):c.1245C>T (p.His415=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 1409974	NM_001382430.1(AKT1):c.1245C>G (p.His415Gln)	AKT1 (H415Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1442307	NM_001382430.1(AKT1):c.1243C>T (p.His415Tyr)	AKT1 (H415Y)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 473851	NM_001382430.1(AKT1):c.1242G>C (p.Gln414His)	AKT1 (Q414H)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 950518	NM_001382430.1(AKT1):c.1234G>A (p.Val412Met)	AKT1 (V412M)	Single nucleotide variant (missense variant)	Cowden syndrome 6 +1 more	GUncertain significance
Select item 240106	NM_001382430.1(AKT1):c.1233C>T (p.Ile411=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +2 more	GLikely benign
Select item 240105	NM_001382430.1(AKT1):c.1228G>A (p.Gly410Ser)	AKT1 (G410S)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 240104	NM_001382430.1(AKT1):c.1227C>T (p.Ala409=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 2178552	NM_001382430.1(AKT1):c.1217G>A (p.Arg406His)	AKT1 (R406H)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 946214	NM_001382430.1(AKT1):c.1216C>T (p.Arg406Cys)	AKT1 (R406C)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 1667654	NM_001382430.1(AKT1):c.1206C>T (p.Ile402=)	AKT1	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 664530	NM_001382430.1(AKT1):c.1198A>G (p.Lys400Glu)	AKT1 (K400E)	Single nucleotide variant (missense variant)	Cowden syndrome 6 +1 more	GUncertain significance
Select item 640033	NM_001382430.1(AKT1):c.1195G>A (p.Ala399Thr)	AKT1 (A399T)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 473849	NM_001382430.1(AKT1):c.1194C>T (p.Asp398=)	AKT1	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 473848	NM_001382430.1(AKT1):c.1191G>T (p.Glu397Asp)	AKT1 (E397D)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 2869045	NM_001382430.1(AKT1):c.1190A>C (p.Glu397Ala)	AKT1 (E397A)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 1404494	NM_001382430.1(AKT1):c.1189G>A (p.Glu397Lys)	AKT1 (E397K)	Single nucleotide variant (missense variant)	Cowden syndrome 6 +2 more	GUncertain significance
Select item 940930	NM_001382430.1(AKT1):c.1189G>C (p.Glu397Gln)	AKT1 (E397Q)	Single nucleotide variant (missense variant)	Cowden syndrome 6	GUncertain significance
Select item 771610	NM_001382430.1(AKT1):c.1188C>T (p.Ser396=)	AKT1	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 240103	NM_001382430.1(AKT1):c.1179C>T (p.Gly393=)	AKT1	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 1107585	NM_001382430.1(AKT1):c.1176T>C (p.Leu392=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GLikely benign
Select item 999063	NM_001382430.1(AKT1):c.1173G>A (p.Arg391=)	AKT1	Single nucleotide variant (synonymous variant)	Cowden syndrome 6 +1 more	GConflicting classifications of pathogenicity
Select item 1003666	NM_001382430.1(AKT1):c.1173-6C>G	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 2725354	NM_001382430.1(AKT1):c.1173-8G>C	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 2082145	NM_001382430.1(AKT1):c.1173-8G>A	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 2764654	NM_001382430.1(AKT1):c.1173-18C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1604942	NM_001382430.1(AKT1):c.1172+16C>G	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 701686	NM_001382430.1(AKT1):c.1172+10G>A	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1108424	NM_001382430.1(AKT1):c.1172+9C>A	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 702510	NM_001382430.1(AKT1):c.1172+9C>T	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign
Select item 1535833	NM_001382430.1(AKT1):c.1172+7G>A	AKT1	Single nucleotide variant (intron variant)	Cowden syndrome 6	GLikely benign

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