List of variants in gene CHST6 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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_021615.5(CHST6):c.599T>G (p.Leu200Arg)	rs28937879	0.00021
NM_021615.5(CHST6):c.304T>G (p.Cys102Gly)	rs121917822	0.00003
NM_021615.5(CHST6):c.329A>G (p.Tyr110Cys)	rs72547544	0.00001
NM_021615.5(CHST6):c.521A>G (p.Lys174Arg)	rs28937877	0.00001
NM_021615.5(CHST6):c.827T>C (p.Leu276Pro)	rs121917824	0.00001
CHST6, DELETION OF 5-PRIME REGION
CHST6, REPLACEMENT OF 5-PRIME REGION
NM_021615.5(CHST6):c.277C>A (p.Arg93Ser)	rs121917826
NM_021615.5(CHST6):c.609C>A (p.Asp203Glu)	rs28937878

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.