List of variants in gene GIPC3 reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_133261.3(GIPC3):c.4G>A (p.Glu2Lys)	rs764467903	0.00110
NM_133261.3(GIPC3):c.*15G>A	rs368944411	0.00048
NM_133261.3(GIPC3):c.883G>A (p.Glu295Lys)	rs201853780	0.00016
NM_133261.3(GIPC3):c.50C>G (p.Ala17Gly)	rs876657815	0.00014
NM_133261.3(GIPC3):c.-15C>T	rs1214727223	0.00005
NM_133261.3(GIPC3):c.773G>A (p.Arg258Gln)	rs775474512	0.00004
NM_133261.3(GIPC3):c.875T>C (p.Phe292Ser)	rs727503065	0.00003
NM_133261.3(GIPC3):c.271C>T (p.Leu91Phe)	rs1599862314	0.00001
NM_133261.3(GIPC3):c.298G>A (p.Asp100Asn)	rs727503063	0.00001
NM_133261.3(GIPC3):c.545A>C (p.Lys182Thr)	rs904746365	0.00001
NM_133261.3(GIPC3):c.674G>A (p.Arg225His)	rs727503064	0.00001
NM_133261.3(GIPC3):c.245A>G (p.Asn82Ser)	rs747242422
NM_133261.3(GIPC3):c.411+6C>T	rs764713230
NM_133261.3(GIPC3):c.596T>C (p.Met199Thr)	rs1241786174
NM_133261.3(GIPC3):c.939G>C (p.Ter313Tyr)	rs1172324481

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.