List of variants in gene LOC129933707, MSH6 studied for Lynch syndrome 5

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.260+22C>G	rs55927047	0.13136
NM_000179.3(MSH6):c.257C>T (p.Thr86Ile)	rs768444916	0.00002
NM_000179.3(MSH6):c.215_258del (p.Leu72fs)	rs1553408380
NM_000179.3(MSH6):c.249T>G (p.Ala83=)	rs876658308
NM_000179.3(MSH6):c.253C>T (p.Pro85Ser)	rs779664343
NM_000179.3(MSH6):c.254CCA[1] (p.Thr86del)	rs1553408448
NM_000179.3(MSH6):c.255C>A (p.Pro85=)	rs587779242
NM_000179.3(MSH6):c.255del (p.Thr86fs)	rs1064793183
NM_000179.3(MSH6):c.260+15del	rs1553408495
NM_000179.3(MSH6):c.260+1G>C	rs1553408467
NM_000179.3(MSH6):c.260+2T>C	rs1553408469
NM_000179.3(MSH6):c.260+2T>G
NM_000179.3(MSH6):c.260+2_260+3delinsAG	rs1064794075

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.