List of variants in gene combination EPHB4, LOC126860124 reported as uncertain significance for capillary malformation-arteriovenous malformation syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004444.5(EPHB4):c.2365C>T (p.Pro789Ser)	rs1417508111	0.00003
NM_004444.5(EPHB4):c.2366C>G (p.Pro789Arg)	rs753075600
NM_004444.5(EPHB4):c.2419G>A (p.Gly807Arg)	rs1330628156
NM_004444.5(EPHB4):c.2458C>A (p.Pro820Thr)	rs1584653653
NM_004444.5(EPHB4):c.2459C>T (p.Pro820Leu)	rs1584653650
NM_004444.5(EPHB4):c.2475C>T (p.Ser825=)
NM_004444.5(EPHB4):c.2567G>A (p.Cys856Tyr)	rs1584653005
NM_004444.5(EPHB4):c.2609T>A (p.Val870Glu)	rs1584652920
NM_004444.5(EPHB4):c.2621T>C (p.Leu874Pro)	rs1584652900

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.