Related gene-specific medical variations for Gene (Select 63977) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3309768	NM_001040424.3(PRDM15):c.1936A>G (p.Met646Val)	LOC126653385, PRDM15 (M666V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309762	NM_001040424.3(PRDM15):c.323C>T (p.Thr108Ile)	LOC126653386, PRDM15 (T108I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309756	NM_001040424.3(PRDM15):c.1862C>T (p.Ser621Leu)	LOC126653385, PRDM15 (S641L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218377	NM_001040424.3(PRDM15):c.1804G>A (p.Gly602Ser)	LOC126653385, PRDM15 (G602S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652691	NM_001040424.3(PRDM15):c.318C>T (p.Phe106=)	LOC126653386, PRDM15	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2652690	NM_001040424.3(PRDM15):c.520G>A (p.Ala174Thr)	LOC126653386, PRDM15 (A174T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2542963	NM_001040424.3(PRDM15):c.2029C>T (p.Arg677Cys)	LOC126653385, PRDM15 (R677C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470342	NM_001040424.3(PRDM15):c.1801A>G (p.Ile601Val)	LOC126653385, PRDM15 (I621V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457575	NM_001040424.3(PRDM15):c.308C>G (p.Pro103Arg)	LOC126653386, PRDM15 (P103R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363282	NM_001040424.3(PRDM15):c.310G>A (p.Val104Met)	LOC126653386, PRDM15 (V104M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362455	NM_001040424.3(PRDM15):c.1832A>C (p.Asn611Thr)	LOC126653385, PRDM15 (N611T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342198	NM_001040424.3(PRDM15):c.415G>A (p.Asp139Asn)	LOC126653386, PRDM15 (D205N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314308	NM_001040424.3(PRDM15):c.1768G>C (p.Ala590Pro)	LOC126653385, PRDM15 (A590P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance