List of variants in gene SGCB reported by CeGaT Center for Human Genetics Tuebingen

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: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000232.5(SGCB):c.*2907T>C	rs138349341	0.00486
NM_000232.5(SGCB):c.943G>A (p.Gly315Arg)	rs150395645	0.00041
NM_000232.5(SGCB):c.151C>T (p.Arg51Cys)	rs144743676	0.00029
NM_000232.5(SGCB):c.496A>G (p.Ile166Val)	rs138877636	0.00028
NM_000232.5(SGCB):c.495C>T (p.Asp165=)	rs142801720	0.00025
NM_000232.5(SGCB):c.341C>T (p.Ser114Phe)	rs150518260	0.00019
NM_000232.5(SGCB):c.799C>T (p.Arg267Cys)	rs200761715	0.00012
NM_000232.5(SGCB):c.833G>A (p.Gly278Asp)	rs777817786	0.00004
NM_000232.5(SGCB):c.939C>T (p.Pro313=)	rs375438506	0.00004
NM_000232.5(SGCB):c.551A>G (p.Tyr184Cys)	rs1365923535	0.00002
NM_000232.5(SGCB):c.544A>C (p.Thr182Pro)	rs751427686	0.00001
NM_000232.5(SGCB):c.504_505delinsAG (p.Met168_Gln169delinsIleGlu)	rs2109371031

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.