"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "TBC1D32 - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2758665	NM_152730.6(TBC1D32):c.3749G>A (p.Arg1250Gln)	TBC1D32 (R1291Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2009950	NM_152730.6(TBC1D32):c.3713A>G (p.Glu1238Gly)	TBC1D32 (E1279G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1383946	NM_152730.6(TBC1D32):c.3711G>A (p.Leu1237=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 1541792	NM_152730.6(TBC1D32):c.3695A>C (p.Glu1232Ala)	TBC1D32 (E1232A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 781887	NM_152730.6(TBC1D32):c.3667C>T (p.His1223Tyr)	TBC1D32 (H1223Y +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2747244	NM_152730.6(TBC1D32):c.3614T>C (p.Leu1205Pro)	TBC1D32 (L1205P +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 782999	NM_152730.6(TBC1D32):c.3539C>T (p.Thr1180Ile)	TBC1D32 (T1180I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2547813	NM_152730.6(TBC1D32):c.3527A>G (p.His1176Arg)	TBC1D32 (H1176R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 764534	NM_152730.6(TBC1D32):c.3510T>C (p.Asp1170=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2727306	NM_152730.6(TBC1D32):c.3466-6_3466-5dup	TBC1D32	Duplication (intron variant)	not provided	GBenign
Select item 1560532	NM_152730.6(TBC1D32):c.3466-5dup	TBC1D32	Duplication (intron variant)	not provided	GBenign
Select item 1601435	NM_152730.6(TBC1D32):c.3466-5del	TBC1D32	Deletion (intron variant)	not provided	GBenign
Select item 2720437	NM_152730.6(TBC1D32):c.3446C>T (p.Ser1149Phe)	TBC1D32 (S1190F +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 737222	NM_152730.6(TBC1D32):c.3424G>T (p.Val1142Leu)	TBC1D32 (V1142L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2132826	NM_152730.6(TBC1D32):c.3384C>A (p.Thr1128=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 742756	NM_152730.6(TBC1D32):c.3372T>C (p.Tyr1124=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1600966	NM_152730.6(TBC1D32):c.3351A>G (p.Glu1117=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 790586	NM_152730.6(TBC1D32):c.3333T>G (p.Leu1111=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1366956	NM_152730.6(TBC1D32):c.3311G>C (p.Arg1104Thr)	TBC1D32 (R1145T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 744746	NM_152730.6(TBC1D32):c.3201C>T (p.Asp1067=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 795870	NM_152730.6(TBC1D32):c.3189T>C (p.Tyr1063=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2178169	NM_152730.6(TBC1D32):c.3131T>C (p.Phe1044Ser)	TBC1D32 (F1044S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2054643	NM_152730.6(TBC1D32):c.3107G>A (p.Trp1036Ter)	TBC1D32 (W1077* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2860585	NM_152730.6(TBC1D32):c.3099T>C (p.Asp1033=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1587392	NM_152730.6(TBC1D32):c.3088G>T (p.Ala1030Ser)	TBC1D32 (A1030S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1924080	NM_152730.6(TBC1D32):c.3078A>G (p.Leu1026=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1599145	NM_152730.6(TBC1D32):c.3053+20C>T	TBC1D32	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 744429	NM_152730.6(TBC1D32):c.3053+9T>A	TBC1D32	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2761243	NM_152730.6(TBC1D32):c.3026A>G (p.Gln1009Arg)	TBC1D32 (Q1009R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1897050	NM_152730.6(TBC1D32):c.2983+19G>A	TBC1D32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1932446	NM_152730.6(TBC1D32):c.2978A>C (p.Tyr993Ser)	TBC1D32 (Y993S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2978364	NM_152730.6(TBC1D32):c.2956T>C (p.Cys986Arg)	TBC1D32 (C1027R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1395650	NM_152730.6(TBC1D32):c.2951C>G (p.Ser984Cys)	TBC1D32 (S1025C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 751718	NM_152730.6(TBC1D32):c.2799A>G (p.Leu933=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1600111	NM_152730.6(TBC1D32):c.2775C>T (p.Asp925=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1904835	NM_152730.6(TBC1D32):c.2751A>G (p.Thr917=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1937603	NM_152730.6(TBC1D32):c.2744A>G (p.Asp915Gly)	TBC1D32 (D915G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1987636	NM_152730.6(TBC1D32):c.2734T>A (p.Tyr912Asn)	TBC1D32 (Y953N +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2120267	NM_152730.6(TBC1D32):c.2699G>T (p.Trp900Leu)	TBC1D32 (W941L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2055847	NM_152730.6(TBC1D32):c.2680-3del	TBC1D32	Deletion (intron variant)	not provided	GBenign
Select item 1992112	NM_152730.6(TBC1D32):c.2678A>T (p.Lys893Met)	TBC1D32 (K893M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 771404	NM_152730.6(TBC1D32):c.2664G>A (p.Pro888=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 708436	NM_152730.6(TBC1D32):c.2663C>T (p.Pro888Leu)	TBC1D32 (P929L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1375536	NM_152730.6(TBC1D32):c.2651G>A (p.Arg884Gln)	TBC1D32 (R884Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2359489	NM_152730.6(TBC1D32):c.2586T>A (p.Asp862Glu)	TBC1D32 (D903E +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2001657	NM_152730.6(TBC1D32):c.2482-8T>A	TBC1D32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1506005	NM_152730.6(TBC1D32):c.2458C>T (p.Arg820Cys)	TBC1D32 (R820C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2109728	NM_152730.6(TBC1D32):c.2433T>C (p.Leu811=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1559260	NM_152730.6(TBC1D32):c.2431C>A (p.Leu811Ile)	TBC1D32 (L811I)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1381835	NM_152730.6(TBC1D32):c.2429A>T (p.Asp810Val)	TBC1D32 (D810V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1972323	NM_152730.6(TBC1D32):c.2270A>C (p.Glu757Ala)	TBC1D32 (E757A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1579717	NM_152730.6(TBC1D32):c.2245+16T>G	TBC1D32	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1933353	NM_152730.6(TBC1D32):c.2245+10T>A	TBC1D32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2713241	NM_152730.6(TBC1D32):c.2225G>A (p.Gly742Asp)	TBC1D32 (G742D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 724958	NM_152730.6(TBC1D32):c.2215G>A (p.Ala739Thr)	TBC1D32 (A739T)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1598848	NM_152730.6(TBC1D32):c.2158-19T>A	TBC1D32	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 788413	NM_152730.6(TBC1D32):c.2070C>A (p.Thr690=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2032926	NM_152730.6(TBC1D32):c.2065G>A (p.Ala689Thr)	TBC1D32 (A689T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 761642	NM_152730.6(TBC1D32):c.2061T>C (p.Phe687=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1927835	NM_152730.6(TBC1D32):c.2019-9C>T	TBC1D32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2189117	NM_152730.6(TBC1D32):c.2018+10A>G	TBC1D32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1524237	NM_152730.6(TBC1D32):c.1982A>T (p.Asp661Val)	TBC1D32 (D661V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 709415	NM_152730.6(TBC1D32):c.1974G>C (p.Glu658Asp)	TBC1D32 (E658D)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 709826	NM_152730.6(TBC1D32):c.1895C>T (p.Thr632Ile)	TBC1D32 (T632I)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2021587	NM_152730.6(TBC1D32):c.1866T>C (p.Ser622=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1544398	NM_152730.6(TBC1D32):c.1795A>G (p.Ile599Val)	TBC1D32 (I599V)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2713331	NM_152730.6(TBC1D32):c.1779C>T (p.Leu593=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1535606	NM_152730.6(TBC1D32):c.1734-11T>C	TBC1D32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1591226	NM_152730.6(TBC1D32):c.1734-14G>A	TBC1D32	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1586237	NM_152730.6(TBC1D32):c.1733+20C>T	TBC1D32	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2810441	NM_152730.6(TBC1D32):c.1642C>T (p.His548Tyr)	TBC1D32 (H548Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1516688	NM_152730.6(TBC1D32):c.1609G>T (p.Ala537Ser)	TBC1D32 (A537S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2077878	NM_152730.6(TBC1D32):c.1561A>G (p.Ile521Val)	TBC1D32 (I521V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1966483	NM_152730.6(TBC1D32):c.1538A>T (p.Glu513Val)	TBC1D32 (E513V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1588690	NM_152730.6(TBC1D32):c.1513A>T (p.Ser505Cys)	TBC1D32 (S505C)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1599516	NM_152730.6(TBC1D32):c.1503G>A (p.Leu501=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2054812	NM_152730.6(TBC1D32):c.1466A>T (p.Glu489Val)	TBC1D32 (E489V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1905306	NM_152730.6(TBC1D32):c.1459C>T (p.His487Tyr)	LOC132089326, TBC1D32 (H487Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2079307	NM_152730.6(TBC1D32):c.1433G>A (p.Ser478Asn)	LOC132089326, TBC1D32 (S478N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 792051	NM_152730.6(TBC1D32):c.1288A>C (p.Ile430Leu)	TBC1D32 (I430L)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1448407	NM_152730.6(TBC1D32):c.1279A>G (p.Ile427Val)	TBC1D32 (I427V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1629549	NM_152730.6(TBC1D32):c.1231+15_1231+18del	TBC1D32	Deletion (intron variant)	not provided	GLikely benign
Select item 1629550	NM_152730.6(TBC1D32):c.1231+13_1231+14delinsAG	TBC1D32	Indel (intron variant)	not provided	GLikely benign
Select item 1935093	NM_152730.6(TBC1D32):c.1184G>A (p.Cys395Tyr)	TBC1D32 (C395Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2190814	NM_152730.6(TBC1D32):c.1143A>G (p.Val381=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1301430	NM_152730.6(TBC1D32):c.1141-20A>G	TBC1D32	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1600256	NM_152730.6(TBC1D32):c.1124C>A (p.Thr375Lys)	TBC1D32 (T375K)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2186905	NM_152730.6(TBC1D32):c.1046T>A (p.Val349Asp)	TBC1D32 (V349D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1905840	NM_152730.6(TBC1D32):c.1026G>C (p.Pro342=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 760605	NM_152730.6(TBC1D32):c.996C>T (p.Ser332=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3021327	NM_152730.6(TBC1D32):c.976A>G (p.Thr326Ala)	TBC1D32 (T326A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1987650	NM_152730.6(TBC1D32):c.935+19T>C	TBC1D32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1988109	NM_152730.6(TBC1D32):c.935+12C>T	TBC1D32	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1613557	NM_152730.6(TBC1D32):c.935+8C>T	TBC1D32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2973334	NM_152730.6(TBC1D32):c.922C>T (p.Arg308Cys)	TBC1D32 (R308C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2105028	NM_152730.6(TBC1D32):c.874-16G>A	TBC1D32	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2044065	NM_152730.6(TBC1D32):c.860G>A (p.Arg287His)	TBC1D32 (R287H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1511118	NM_152730.6(TBC1D32):c.859C>T (p.Arg287Cys)	TBC1D32 (R287C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 757718	NM_152730.6(TBC1D32):c.852T>C (p.Asn284=)	TBC1D32	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 716029	NM_152730.6(TBC1D32):c.838A>G (p.Ile280Val)	TBC1D32 (I280V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign

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