Related gene-specific medical variations for Gene (Select 101929064) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3123218	NM_138982.4(MAPK10):c.95A>T (p.Tyr32Phe)	MAPK10, MAPK10-AS1 (Y32F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3123216	NM_138982.4(MAPK10):c.20A>G (p.Tyr7Cys)	MAPK10, MAPK10-AS1 (Y7C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3123214	NM_138982.4(MAPK10):c.121A>C (p.Lys41Gln)	MAPK10, MAPK10-AS1 (K3Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 793018	NM_138982.4(MAPK10):c.24C>T (p.Tyr8=)	MAPK10, MAPK10-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 211433	NM_138982.4(MAPK10):c.21C>A (p.Tyr7Ter)	MAPK10, MAPK10-AS1 (Y7*)	Single nucleotide variant (nonsense +1 more)	not specified	GUncertain significance

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