List of variants in gene LAMB3 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000228.3(LAMB3):c.1903C>T (p.Arg635Ter)	rs80356682	0.00049
NM_000228.3(LAMB3):c.124C>T (p.Arg42Ter)	rs80356680	0.00006
NM_000228.3(LAMB3):c.628+42G>A	rs587776812	0.00001
NM_000228.3(LAMB3):c.628G>A (p.Glu210Lys)	rs121912482	0.00001
NM_000228.3(LAMB3):c.1439_1443del (p.Pro480fs)	rs786205095
NM_000228.3(LAMB3):c.1587_1588del (p.Gly530fs)	rs769151482
NM_000228.3(LAMB3):c.1830G>A (p.Trp610Ter)	rs121912484
NM_000228.3(LAMB3):c.2806C>T (p.Gln936Ter)	rs121912485
NM_000228.3(LAMB3):c.3394dup (p.Glu1132fs)	rs786201004
NM_000228.3(LAMB3):c.3431C>A (p.Ser1144Ter)	rs869320671
NM_000228.3(LAMB3):c.3446_3453del (p.Gly1149fs)	rs1553275034
NM_000228.3(LAMB3):c.496C>T (p.Gln166Ter)	rs121912483
NM_000228.3(LAMB3):c.565-3T>C	rs587776813
NM_000228.3(LAMB3):c.596G>C (p.Gly199Ala)	rs121912486
NM_000228.3(LAMB3):c.619A>C (p.Lys207Gln)	rs121912487
NM_000228.3(LAMB3):c.629-1G>A	rs587776814
NM_000228.3(LAMB3):c.904del (p.Trp302fs)	rs786205094

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.