Related gene-specific medical variations for Gene (Select 23532) - ClinVar

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Links from Gene

Items: 43

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3309663	NM_206956.3(PRAME):c.1293C>G (p.Ile431Met)	IGL, PRAME (I415M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309662	NM_206956.3(PRAME):c.130G>A (p.Ala44Thr)	IGL, PRAME (A28T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218133	NM_206956.3(PRAME):c.998G>A (p.Arg333Gln)	IGL, PRAME (R317Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218132	NM_206956.3(PRAME):c.833C>T (p.Pro278Leu)	IGL, PRAME (P262L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218131	NM_206956.3(PRAME):c.82G>A (p.Glu28Lys)	IGL, PRAME (E12K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218130	NM_206956.3(PRAME):c.770G>A (p.Gly257Asp)	IGL, PRAME (G257D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218129	NM_206956.3(PRAME):c.697G>T (p.Asp233Tyr)	IGL, PRAME (D217Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218128	NM_206956.3(PRAME):c.654G>T (p.Met218Ile)	IGL, PRAME (M202I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218127	NM_206956.3(PRAME):c.362T>C (p.Val121Ala)	IGL, PRAME (V105A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218126	NM_206956.3(PRAME):c.1465C>T (p.His489Tyr)	IGL, PRAME (H489Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218125	NM_206956.3(PRAME):c.1426C>T (p.Arg476Trp)	IGL, PRAME (R460W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218124	NM_206956.3(PRAME):c.1304A>G (p.Asn435Ser)	IGL, PRAME (N435S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218123	NM_206956.3(PRAME):c.1020G>A (p.Met340Ile)	IGL, PRAME (M340I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3218122	NM_206956.3(PRAME):c.1009G>C (p.Gly337Arg)	IGL, PRAME (G321R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622658	NM_206956.3(PRAME):c.92G>T (p.Gly31Val)	IGL, PRAME (G31V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591552	NM_206956.3(PRAME):c.1510C>T (p.Pro504Ser)	IGL, PRAME (P504S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535753	NM_206956.3(PRAME):c.1361C>G (p.Thr454Ser)	IGL, PRAME (T454S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526556	NM_206956.3(PRAME):c.967C>G (p.Pro323Ala)	IGL, PRAME (P307A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512782	NM_206956.3(PRAME):c.236C>T (p.Thr79Ile)	IGL, PRAME (T63I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457337	NM_206956.3(PRAME):c.374G>A (p.Arg125Gln)	IGL, PRAME (R109Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410473	NM_206956.3(PRAME):c.1004C>T (p.Ser335Leu)	IGL, PRAME (S335L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408485	NM_206956.3(PRAME):c.692A>G (p.Gln231Arg)	IGL, PRAME (Q231R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401473	NM_206956.3(PRAME):c.1016T>C (p.Val339Ala)	IGL, PRAME (V323A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394902	NM_206956.3(PRAME):c.1408T>G (p.Leu470Val)	IGL, PRAME (L470V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391635	NM_206956.3(PRAME):c.1078A>C (p.Met360Leu)	IGL, PRAME (M360L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382435	NM_206956.3(PRAME):c.514T>G (p.Phe172Val)	IGL, PRAME (F156V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361050	NM_206956.3(PRAME):c.749C>T (p.Ala250Val)	IGL, PRAME (A234V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321373	NM_206956.3(PRAME):c.1513T>C (p.Cys505Arg)	IGL, PRAME (C489R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318608	NM_206956.3(PRAME):c.1172C>T (p.Thr391Met)	IGL, PRAME (T375M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2315032	NM_206956.3(PRAME):c.124A>G (p.Ile42Val)	IGL, PRAME (I26V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295908	NM_206956.3(PRAME):c.794T>G (p.Leu265Arg)	IGL, PRAME (L265R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285894	NM_206956.3(PRAME):c.562T>C (p.Cys188Arg)	IGL, PRAME (C188R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246548	NM_206956.3(PRAME):c.337C>T (p.Arg113Cys)	IGL, PRAME (R97C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238876	NM_206956.3(PRAME):c.403G>A (p.Val135Ile)	IGL, PRAME (V135I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233100	NM_206956.3(PRAME):c.796C>T (p.Leu266Phe)	IGL, PRAME (L266F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225287	NM_206956.3(PRAME):c.671A>G (p.Lys224Arg)	IGL, PRAME (K224R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220089	NM_206956.3(PRAME):c.1377G>T (p.Arg459Ser)	IGL, PRAME (R443S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215112	NM_206956.3(PRAME):c.958G>T (p.Val320Leu)	IGL, PRAME (V304L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2205518	NM_206956.3(PRAME):c.1078A>G (p.Met360Val)	IGL, PRAME (M360V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1296948	NM_206956.3(PRAME):c.19T>C (p.Trp7Arg)	IGL, PRAME (W7R)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 782671	NM_206956.3(PRAME):c.611A>G (p.Asn204Ser)	IGL, PRAME (N204S +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 778915	NM_206956.3(PRAME):c.766C>T (p.Leu256=)	IGL, PRAME	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 777670	NM_206956.3(PRAME):c.1263T>C (p.Ser421=)	IGL, PRAME	Single nucleotide variant (synonymous variant)	not provided	GBenign

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Links from Gene

Items: 43