ClinVar for Gene (Select 54209) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3061615	NM_018965.4(TREM2):c.*2G>A	TREM2	Single nucleotide variant (synonymous variant +1 more)	TREM2-related condition	GLikely benign
Select item 3054123	NM_018965.4(TREM2):c.432C>T (p.Pro144=)	TREM2	Single nucleotide variant (synonymous variant)	TREM2-related condition	GLikely benign
Select item 3050499	NM_018965.4(TREM2):c.417A>C (p.Gly139=)	TREM2	Single nucleotide variant (synonymous variant)	TREM2-related condition	GLikely benign
Select item 3034609	NM_018965.4(TREM2):c.*169G>A	TREM2	Single nucleotide variant (3 prime UTR variant)	TREM2-related condition	GLikely benign
Select item 3012919	NM_018965.4(TREM2):c.368del (p.Lys123fs)	TREM2 (K123fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 3012356	NM_018965.4(TREM2):c.291G>A (p.Leu97=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2999468	NM_018965.4(TREM2):c.41-18T>C	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2995806	NM_018965.4(TREM2):c.408G>T (p.Arg136=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2975372	NM_018965.4(TREM2):c.534C>A (p.Leu178=)	TREM2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2961094	NM_018965.4(TREM2):c.424T>C (p.Trp142Arg)	TREM2 (W142R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2957437	NM_018965.4(TREM2):c.288G>T (p.Thr96=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2910198	NM_018965.4(TREM2):c.198G>A (p.Thr66=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2879867	NM_018965.4(TREM2):c.147C>T (p.Ala49=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2858468	NM_018965.4(TREM2):c.174C>G (p.Gly58=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2824995	NM_018965.4(TREM2):c.40+7T>C	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2800377	NM_018965.4(TREM2):c.102G>A (p.Val34=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2715444	NM_018965.4(TREM2):c.392-2A>T	TREM2	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 2703277	NM_018965.4(TREM2):c.54C>T (p.Ala18=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2693499	NM_018965.4(TREM2):c.256_265del (p.Asp86fs)	TREM2 (D86fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2685202	GRCh37/hg19 6p21.31-21.1(chr6:35562152-42003452)x1	BNIP5, APOBEC2 +67 more	Copy number loss	not provided	GPathogenic
Select item 2583155	NM_018965.4(TREM2):c.40+1G>A	TREM2	Single nucleotide variant (splice donor variant)	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2	GPathogenic
Select item 2573593	NM_018965.4(TREM2):c.22A>T (p.Ile8Phe)	TREM2 (I8F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2573592	NM_018965.4(TREM2):c.41-20AATG[3]	TREM2	Microsatellite (intron variant)	not specified	GUncertain significance
Select item 2551019	NM_018965.4(TREM2):c.55C>A (p.His19Asn)	TREM2 (H19N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2437259	NM_018965.4(TREM2):c.203A>T (p.Asn68Ile)	TREM2 (N68I)	Single nucleotide variant (missense variant)	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2	GUncertain significance
Select item 2426502	NC_000006.11:g.(?_41126341)_(41130820_?)del	TREM2	Deletion	not provided	GPathogenic
Select item 2422887	NC_000006.11:g.(?_41126341)_(43737486_?)dup	BYSL, ABCC10 +57 more	Duplication	PRPH2-Related Disorders	GUncertain significance
Select item 2422814	NC_000006.11:g.(?_41126341)_(43752536_?)del	ABCC10, BICRAL +58 more	Deletion	Peroxisome biogenesis disorder	GPathogenic
Select item 2374599	NM_018965.4(TREM2):c.79G>A (p.Val27Met)	TREM2 (V27M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2323909	NM_018965.4(TREM2):c.304C>A (p.Pro102Thr)	TREM2 (P102T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2288192	NM_018965.4(TREM2):c.433G>A (p.Gly145Arg)	TREM2 (G145R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2287139	NM_018965.4(TREM2):c.49G>A (p.Gly17Arg)	TREM2 (G17R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2178794	NM_018965.4(TREM2):c.482+8G>A	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2136385	NM_018965.4(TREM2):c.155G>A (p.Arg52His)	TREM2 (R52H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2135653	NM_018965.4(TREM2):c.*101G>C	TREM2 (W200C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2131026	NM_018965.4(TREM2):c.*26A>G	TREM2	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2113791	NM_018965.4(TREM2):c.260A>T (p.Asp87Val)	TREM2 (D87V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2108683	NM_018965.4(TREM2):c.*53A>T	TREM2	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2101108	NM_018965.4(TREM2):c.219C>A (p.Ser73=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2090028	NM_018965.4(TREM2):c.200A>G (p.His67Arg)	TREM2 (H67R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2076802	NM_018965.4(TREM2):c.152G>A (p.Cys51Tyr)	TREM2 (C51Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2070342	NM_018965.4(TREM2):c.172G>A (p.Gly58Ser)	TREM2 (G58S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2020997	NM_018965.4(TREM2):c.513A>C (p.Pro171=)	TREM2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1995957	NM_018965.4(TREM2):c.463G>A (p.Val155Met)	TREM2 (V155M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1993730	NM_018965.4(TREM2):c.*45A>G	TREM2 (T182A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1991458	NM_018965.4(TREM2):c.462T>C (p.His154=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1984734	NM_018965.4(TREM2):c.269G>A (p.Gly90Asp)	TREM2 (G90D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1982815	NM_018965.4(TREM2):c.538G>C (p.Ala180Pro)	TREM2 (A180P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1973298	NM_018965.4(TREM2):c.434G>C (p.Gly145Ala)	TREM2 (G145A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1969696	NM_018965.4(TREM2):c.482+16T>C	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1966298	NM_018965.4(TREM2):c.*61T>C	TREM2 (I187T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1965316	NM_018965.4(TREM2):c.369G>A (p.Lys123=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1963201	NM_018965.4(TREM2):c.134G>A (p.Gly45Glu)	TREM2 (G45E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1959798	NM_018965.4(TREM2):c.*102C>G	TREM2 (Q201E)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1954186	NM_018965.4(TREM2):c.*105G>C	TREM2 (E202Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1945329	NM_018965.4(TREM2):c.*123C>T	TREM2 (H208Y)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1935382	NM_018965.4(TREM2):c.175C>G (p.Pro59Ala)	TREM2 (P59A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1928303	NM_018965.4(TREM2):c.432C>G (p.Pro144=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1919056	NM_018965.4(TREM2):c.*70C>T	TREM2 (T190I)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1912125	NM_018965.4(TREM2):c.471C>T (p.His157=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1909743	NM_018965.4(TREM2):c.145G>T (p.Ala49Ser)	TREM2 (A49S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1908467	NM_018965.4(TREM2):c.41-17G>A	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1897638	NM_018965.4(TREM2):c.40+15G>A	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1879660	NM_018965.4(TREM2):c.507C>T (p.Pro169=)	TREM2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1706662	NM_018965.4(TREM2):c.483-152C>T	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1701502	NM_018965.4(TREM2):c.675A>G (p.Pro225=)	TREM2	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 1676016	NM_018965.4(TREM2):c.199del (p.His67fs)	TREM2 (H67fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1669903	NM_018965.4(TREM2):c.198G>C (p.Thr66=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1666503	NM_018965.4(TREM2):c.429C>T (p.Phe143=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1664818	NM_018965.4(TREM2):c.292C>A (p.Arg98=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1636146	NM_018965.4(TREM2):c.391+20C>T	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1630841	NM_018965.4(TREM2):c.84G>A (p.Ala28=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1603446	NM_018965.4(TREM2):c.391+14G>A	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1584951	NM_018965.4(TREM2):c.40+8C>G	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1575653	NM_018965.4(TREM2):c.*114C>T	TREM2	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1570242	NM_018965.4(TREM2):c.450C>T (p.Phe150=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1545320	NM_018965.4(TREM2):c.40+14C>T	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1537134	NM_018965.4(TREM2):c.48C>G (p.Ser16=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1536190	NM_018965.4(TREM2):c.392-15C>G	TREM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1534302	NM_018965.4(TREM2):c.*80A>T	TREM2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1517663	NM_018965.4(TREM2):c.451G>A (p.Glu151Lys)	TREM2 (E151K)	Single nucleotide variant (missense variant)	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2 +2 more	GUncertain significance
Select item 1514569	NM_018965.4(TREM2):c.353C>A (p.Ala118Asp)	TREM2 (A118D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1511527	NM_018965.4(TREM2):c.406C>T (p.Arg136Trp)	TREM2 (R136W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1508060	NM_018965.4(TREM2):c.107_108delinsAG	TREM2 (T203A)	Indel (missense variant +1 more)	not provided	GUncertain significance
Select item 1504655	NM_018965.4(TREM2):c.645T>G (p.His215Gln)	TREM2 (H215Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1498893	NM_018965.4(TREM2):c.483-1G>A	TREM2	Single nucleotide variant (intron variant +1 more)	not provided	GLikely pathogenic
Select item 1497089	NM_018965.4(TREM2):c.315G>A (p.Ala105=)	TREM2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1482828	NM_018965.4(TREM2):c.*109C>G	TREM2 (T203S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1473898	NM_018965.4(TREM2):c.483-2A>C	TREM2	Single nucleotide variant (splice acceptor variant +1 more)	not provided	GLikely pathogenic
Select item 1464436	NM_018965.4(TREM2):c.486C>G (p.Ser162Arg)	TREM2 (S162R)	Single nucleotide variant (missense variant +1 more)	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2 +1 more	GUncertain significance
Select item 1448028	NM_018965.4(TREM2):c.287C>T (p.Thr96Met)	TREM2 (T96M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1447460	NM_018965.4(TREM2):c.677-10A>G	TREM2	Single nucleotide variant (intron variant)	TREM2-related condition +1 more	GLikely benign
Select item 1444592	NM_018965.4(TREM2):c.290T>C (p.Leu97Pro)	TREM2 (L97P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1441047	NM_018965.4(TREM2):c.140G>T (p.Arg47Leu)	TREM2 (R47L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1439874	NM_018965.4(TREM2):c.*43G>C	TREM2 (G181A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1430279	NM_018965.4(TREM2):c.433G>T (p.Gly145Trp)	TREM2 (G145W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1412934	NM_018965.4(TREM2):c.*45A>T	TREM2 (T182S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1409635	NM_018965.4(TREM2):c.689C>T (p.Thr230Met)	TREM2 (T230M)	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 1405143	NM_018965.4(TREM2):c.184C>T (p.Arg62Cys)	TREM2 (R62C)	Single nucleotide variant (missense variant)	TREM2-related condition +1 more	GUncertain significance
Select item 1398978	NM_018965.4(TREM2):c.323A>G (p.Tyr108Cys)	TREM2 (Y108C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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