List of variants in gene combination CD3G, LOC126861358 reported as likely benign for immune system disorder

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: 28

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000073.3(CD3G):c.158T>C (p.Ile53Thr)	rs142915569	0.00148
NM_000073.3(CD3G):c.307+13C>T	rs201964905	0.00009
NM_000073.3(CD3G):c.439+12C>T	rs200093444	0.00007
NM_000073.3(CD3G):c.308-13C>T	rs200405767	0.00006
NM_000073.3(CD3G):c.219T>C (p.Asn73=)	rs777518839	0.00002
NM_000073.3(CD3G):c.114A>G (p.Glu38=)	rs751425758	0.00001
NM_000073.3(CD3G):c.381C>T (p.Phe127=)	rs771971617	0.00001
NM_000073.3(CD3G):c.80-17G>A	rs1411479750	0.00001
NM_000073.3(CD3G):c.111A>G (p.Gln37=)
NM_000073.3(CD3G):c.123G>A (p.Ser41=)	rs780567741
NM_000073.3(CD3G):c.162A>C (p.Thr54=)
NM_000073.3(CD3G):c.162A>G (p.Thr54=)
NM_000073.3(CD3G):c.174T>C (p.Asp58=)
NM_000073.3(CD3G):c.189C>T (p.Gly63=)	rs180793518
NM_000073.3(CD3G):c.192C>T (p.Phe64=)
NM_000073.3(CD3G):c.193C>T (p.Leu65=)
NM_000073.3(CD3G):c.231T>C (p.Asn77=)	rs1267984932
NM_000073.3(CD3G):c.243T>C (p.Pro81=)	rs200028255
NM_000073.3(CD3G):c.282A>G (p.Ser94=)
NM_000073.3(CD3G):c.307+18G>A	rs1316251433
NM_000073.3(CD3G):c.307+9T>A
NM_000073.3(CD3G):c.308-10T>G	rs2134070594
NM_000073.3(CD3G):c.308-9T>G	rs2134070596
NM_000073.3(CD3G):c.393T>C (p.Val131=)	rs2134070787
NM_000073.3(CD3G):c.80-10C>T
NM_000073.3(CD3G):c.80-18C>A
NM_000073.3(CD3G):c.80-18C>T	rs771499584
NM_000073.3(CD3G):c.80-19A>G

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.