ClinVar for MedGen (Select 9975) - ClinVar

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

Format

Sort by

Choose Destination

Links from MedGen

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 6263	NM_003921.5(BCL10):c.136del (p.Ile46fs)	BCL10 (I46fs)	Deletion (frameshift variant)	Mesothelioma	GPathogenic
Select item 6250	NM_003921.5(BCL10):c.499dup (p.Ser167fs)	BCL10 (S156fs +1 more)	Duplication (frameshift variant)	Male germ cell tumor, somatic +2 more	GPathogenic
Select item 3499	NM_024426.6(WT1):c.1036A>G (p.Ser346Gly)	WT1 (S129G +7 more)	Single nucleotide variant (missense variant +2 more)	Mesothelioma	GPathogenic

Format

Sort by

Choose Destination