Related gene-specific medical variations for Gene (Select 101928607) - ClinVar - NCBI

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Items: 13

	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 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 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 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 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 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 777552	NM_003307.4(TRPM2):c.3566= (p.Gln1189=)	TRPM2, TRPM2-AS (R1189Q)	Variation (no sequence alteration +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 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