List of variants in gene MSH4 studied for reproductive system disorder

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_002440.4(MSH4):c.2198C>A (p.Ser733Ter)	rs149042353	0.00018
NM_002440.4(MSH4):c.2261C>T (p.Ser754Leu)	rs377712900	0.00005
NM_002440.4(MSH4):c.1540+8C>A
NM_002440.4(MSH4):c.1552C>T (p.Gln518Ter)	rs2100570734
NM_002440.4(MSH4):c.1569T>C (p.Tyr523=)
NM_002440.4(MSH4):c.1575A>T (p.Leu525=)
NM_002440.4(MSH4):c.1782-11_1782-10insAT
NM_002440.4(MSH4):c.1950G>A (p.Trp650Ter)	rs149910287
NM_002440.4(MSH4):c.2179del (p.Asp727fs)	rs2100581757
NM_002440.4(MSH4):c.2222_2225del (p.Lys741fs)	rs1386320504
NM_002440.4(MSH4):c.2355+1G>A	rs774501542
NM_002440.4(MSH4):c.289G>A (p.Ala97Thr)
NM_002440.4(MSH4):c.805_812del (p.Val269fs)	rs2100513927

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.