Related gene-specific medical variations for Gene (Select 79109) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3123342	NM_001006617.3(MAPKAP1):c.1019C>G (p.Thr340Ser)	LOC124310642, MAPKAP1 (T148S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2685363	GRCh37/hg19 9q33.3(chr9:128229678-128283154)x1	MAPKAP1	Copy number loss	not provided	GUncertain significance
Select item 687947	GRCh37/hg19 9q33.3(chr9:128447535-128472084)x1	MAPKAP1	Copy number loss	not provided	GUncertain significance

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