List of variants in gene DCC reported by GeneReviews

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_005215.4(DCC):c.1409G>A (p.Gly470Asp)	rs141813053	0.00296
NM_005215.4(DCC):c.2105A>G (p.Asn702Ser)	rs35691189	0.00284
NM_005215.4(DCC):c.2000G>A (p.Arg667His)	rs200099519	0.00013
NM_005215.4(DCC):c.527A>G (p.Asn176Ser)	rs138724679	0.00011
NM_005215.3(DCC):c.698-?_985+?del (p.Asp233_Leu328del)
NM_005215.4(DCC):c.1140+1G>A	rs797044553
NM_005215.4(DCC):c.1336_1337insAGCC (p.Arg446fs)	rs797044554
NM_005215.4(DCC):c.2407G>A (p.Gly803Arg)	rs797044550
NM_005215.4(DCC):c.2873_2877dup (p.Pro960fs)	rs797044555
NM_005215.4(DCC):c.377C>A (p.Ser126Ter)	rs797044551
NM_005215.4(DCC):c.3836_3837del (p.Leu1279fs)	rs797044556
NM_005215.4(DCC):c.571dup (p.Val191fs)	rs797044552
NM_005215.4(DCC):c.823C>T (p.Arg275Ter)	rs754914260

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.