Related gene-specific medical variations for Gene (Select 5141) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2250239	NM_001111307.2(PDE4A):c.34C>G (p.Leu12Val)	LOC130063497, PDE4A (L12V)	Single nucleotide variant (intron variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 768971	NM_001111307.2(PDE4A):c.60G>C (p.Arg20=)	LOC130063497, PDE4A	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 710380	NM_001111307.2(PDE4A):c.51C>T (p.Pro17=)	LOC130063497, PDE4A	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

Format

Sort by

Choose Destination