List of variants in gene combination HRAS, LRRC56 reported by Fulgent Genetics, Fulgent Genetics

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_005343.4(HRAS):c.357C>T (p.Asp119=)	rs111352454	0.00121
NM_005343.4(HRAS):c.330C>T (p.Pro110=)	rs200747280	0.00011
NM_005343.4(HRAS):c.506G>A (p.Arg169Gln)	rs142218590	0.00007
NM_005343.4(HRAS):c.508A>T (p.Lys170Ter)	rs372936166	0.00005
NM_005343.4(HRAS):c.520C>T (p.Pro174Ser)	rs397517144	0.00004
NM_005343.4(HRAS):c.505C>T (p.Arg169Trp)	rs151229168	0.00003
NM_005343.4(HRAS):c.11A>G (p.Tyr4Cys)	rs764622691	0.00001
NM_005343.4(HRAS):c.410A>C (p.Tyr137Ser)	rs1180561549	0.00001
NM_005343.4(HRAS):c.291-6T>G	rs766909143
NM_005343.4(HRAS):c.34G>T (p.Gly12Cys)	rs104894229
NM_005343.4(HRAS):c.35G>C (p.Gly12Ala)	rs104894230
NM_005343.4(HRAS):c.37G>T (p.Gly13Cys)	rs104894228
NM_005343.4(HRAS):c.38G>A (p.Gly13Asp)	rs104894226
NM_005343.4(HRAS):c.481C>T (p.Arg161Cys)	rs758956556
NM_005343.4(HRAS):c.491G>C (p.Arg164Pro)	rs753977266

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.