Related gene-specific medical variations for Gene (Select 4176) - 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 3124389	NM_005916.5(MCM7):c.19G>A (p.Ala7Thr)	AP4M1, MCM7 (A7T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2294804	NM_005916.5(MCM7):c.27G>T (p.Glu9Asp)	AP4M1, MCM7 (E9D)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1290038	NC_000007.14:g.100101167C>G	AP4M1, MCM7	Single nucleotide variant (intron variant)	not provided	GBenign

Format

Sort by

Choose Destination