Related gene-specific medical variations for Gene (Select 7226) - ClinVar

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Items: 39

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3329209	NM_003307.4(TRPM2):c.3314G>C (p.Arg1105Thr)	TRPM2, TRPM2-AS (R1105T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3329204	NM_003307.4(TRPM2):c.2918A>G (p.His973Arg)	LOC126653395, TRPM2 (H973R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3329203	NM_003307.4(TRPM2):c.2929A>G (p.Thr977Ala)	LOC126653395, TRPM2 (T977A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3183296	NM_003307.4(TRPM2):c.3248C>G (p.Pro1083Arg)	TRPM2, TRPM2-AS (P1083R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3183295	NM_003307.4(TRPM2):c.3238G>A (p.Ala1080Thr)	TRPM2, TRPM2-AS (A1080T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3183291	NM_003307.4(TRPM2):c.2694C>G (p.Ile898Met)	LOC126653395, TRPM2 (I898M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3183290	NM_003307.4(TRPM2):c.2666C>T (p.Pro889Leu)	LOC126653395, TRPM2 (P889L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3183275	NM_003307.4(TRPM2):c.143G>T (p.Cys48Phe)	LOC130066825, TRPM2 (C48F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652751	NM_003307.4(TRPM2):c.2725C>T (p.Arg909Trp)	LOC126653395, TRPM2 (R909W)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2652750	NM_003307.4(TRPM2):c.2669C>T (p.Ala890Val)	LOC126653395, TRPM2 (A890V)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2652749	NM_003307.4(TRPM2):c.2661C>T (p.Leu887=)	LOC126653395, TRPM2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2526793	NM_003307.4(TRPM2):c.2726G>A (p.Arg909Gln)	LOC126653395, TRPM2 (R909Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2478389	NM_003307.4(TRPM2):c.3577T>C (p.Trp1193Arg)	TRPM2, TRPM2-AS (W1243R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402964	NM_003307.4(TRPM2):c.3280A>C (p.Ile1094Leu)	TRPM2, TRPM2-AS (I1094L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377887	NM_003307.4(TRPM2):c.2686C>A (p.Arg896Ser)	LOC126653395, TRPM2 (R896S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374021	NM_003307.4(TRPM2):c.2672C>T (p.Thr891Met)	LOC126653395, TRPM2 (T891M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364261	NM_003307.4(TRPM2):c.2687G>A (p.Arg896His)	LOC126653395, TRPM2 (R896H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2355024	NM_003307.4(TRPM2):c.2689G>A (p.Val897Ile)	LOC126653395, TRPM2 (V897I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2332791	NM_003307.4(TRPM2):c.3174C>G (p.His1058Gln)	TRPM2, TRPM2-AS (H1058Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331939	NM_003307.4(TRPM2):c.151G>A (p.Gly51Ser)	LOC130066825, TRPM2 (G51S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329755	NM_003307.4(TRPM2):c.2881C>T (p.Arg961Cys)	LOC126653395, TRPM2 (R961C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304839	NM_003307.4(TRPM2):c.2881C>G (p.Arg961Gly)	LOC126653395, TRPM2 (R961G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270121	NM_003307.4(TRPM2):c.3173A>C (p.His1058Pro)	TRPM2, TRPM2-AS (H1058P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237670	NM_003307.4(TRPM2):c.2822T>G (p.Leu941Arg)	LOC126653395, TRPM2 (L941R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224750	NM_003307.4(TRPM2):c.2801T>G (p.Val934Gly)	LOC126653395, TRPM2 (V934G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1283778	NM_003307.4(TRPM2):c.2790+55G>A	LOC126653395, TRPM2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274737	NM_003307.4(TRPM2):c.2791-43C>T	LOC126653395, TRPM2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265082	NM_003307.4(TRPM2):c.2791-15C>A	LOC126653395, TRPM2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261780	NM_003307.4(TRPM2):c.3147-20T>C	TRPM2, TRPM2-AS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245588	NM_003307.4(TRPM2):c.3461+194C>T	TRPM2, TRPM2-AS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242396	NM_003307.4(TRPM2):c.3550-134C>T	TRPM2, TRPM2-AS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237695	NM_003307.4(TRPM2):c.2657+319T>G	LOC126653395, TRPM2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 778913	NM_003307.4(TRPM2):c.2790+10C>A	LOC126653395, TRPM2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 777552	NM_003307.4(TRPM2):c.3566= (p.Gln1189=)	TRPM2, TRPM2-AS (R1189Q)	Variation (no sequence alteration +1 more)	not provided	GBenign
Select item 737864	NM_003307.4(TRPM2):c.2857C>T (p.Gln953Ter)	LOC126653395, TRPM2 (Q953*)	Single nucleotide variant (nonsense +1 more)	not provided	GBenign
Select item 726111	NM_003307.4(TRPM2):c.3549+8C>T	TRPM2, TRPM2-AS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 717603	NM_003307.4(TRPM2):c.2658-10C>T	LOC126653395, TRPM2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 715204	NM_003307.4(TRPM2):c.2688C>T (p.Arg896=)	LOC126653395, TRPM2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 596631	NM_003307.4(TRPM2):c.3407G>A (p.Arg1136Gln)	TRPM2, TRPM2-AS (R1136Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

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Links from Gene

Items: 39