Related gene-specific medical variations for Gene (Select 387) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376524	NM_001664.4(RHOA):c.125A>T (p.Tyr42Phe)	RHOA (Y42F)	Single nucleotide variant (missense variant +1 more)	Gastric adenocarcinoma +2 more	GLikely pathogenic
Select item 376523	NM_001664.4(RHOA):c.125A>C (p.Tyr42Ser)	RHOA (Y42S)	Single nucleotide variant (missense variant +1 more)	Gastric adenocarcinoma +2 more	GLikely pathogenic
Select item 376522	NM_001664.4(RHOA):c.125A>G (p.Tyr42Cys)	RHOA (Y42C)	Single nucleotide variant (missense variant +1 more)	Gastric adenocarcinoma +2 more	GLikely pathogenic
Select item 376521	NM_001664.4(RHOA):c.14G>T (p.Arg5Leu)	RHOA (R5L)	Single nucleotide variant (missense variant +1 more)	Non-Hodgkin lymphoma +4 more	GLikely pathogenic
Select item 376520	NM_001664.4(RHOA):c.14G>A (p.Arg5Gln)	RHOA (R5Q)	Single nucleotide variant (missense variant +1 more)	Non-Hodgkin lymphoma +4 more	GLikely pathogenic
Select item 376519	NM_001664.4(RHOA):c.13C>T (p.Arg5Trp)	RHOA (R5W)	Single nucleotide variant (missense variant +1 more)	Carcinoma of esophagus +4 more	GLikely pathogenic
Select item 376518	NM_001664.4(RHOA):c.118G>A (p.Glu40Lys)	RHOA (E40K)	Single nucleotide variant (missense variant +1 more)	Gastric adenocarcinoma +3 more	GLikely pathogenic
Select item 376517	NM_001664.4(RHOA):c.118G>C (p.Glu40Gln)	RHOA (E40Q)	Single nucleotide variant (missense variant +1 more)	Breast neoplasm +3 more	GLikely pathogenic

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