ClinVar Miner

List of variants in gene NLRC5 reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 68
Download table as spreadsheet
HGVS dbSNP
NC_000016.9:g.57023117C>T rs199475962
NC_000016.9:g.57023377C>G rs199475964
NM_001330552.1(NLRC5):c.-1063G>A rs199475960
NM_001330552.1(NLRC5):c.-1074G>A rs199475959
NM_001330552.1(NLRC5):c.-483G>A rs199475963
NM_001330552.1(NLRC5):c.-796C>G rs199475961
NM_032206.4(NLRC5):c.*245C>T rs199476024
NM_032206.4(NLRC5):c.*285C>T rs199476025
NM_032206.4(NLRC5):c.*3G>A rs199476023
NM_032206.4(NLRC5):c.-12-157T>C rs199475965
NM_032206.4(NLRC5):c.1625C>A (p.Thr542Asn) rs199475974
NM_032206.4(NLRC5):c.2009A>C (p.Asp670Ala) rs199475975
NM_032206.4(NLRC5):c.2075+113A>G rs199475976
NM_032206.4(NLRC5):c.2075+154T>C rs199475977
NM_032206.4(NLRC5):c.2076-29C>T rs199475978
NM_032206.4(NLRC5):c.2418-199T>A rs199475980
NM_032206.4(NLRC5):c.2418-213C>T rs199475979
NM_032206.4(NLRC5):c.2477+34T>C rs199475981
NM_032206.4(NLRC5):c.2477+55C>G rs199475982
NM_032206.4(NLRC5):c.2712-121G>C rs199475983
NM_032206.4(NLRC5):c.2712-34C>T rs199475984
NM_032206.4(NLRC5):c.2754G>A (p.Val918=) rs199475985
NM_032206.4(NLRC5):c.2870+353T>C rs199475986
NM_032206.4(NLRC5):c.2871-27A>C rs199475987
NM_032206.4(NLRC5):c.2940-161G>A rs199475988
NM_032206.4(NLRC5):c.2947C>G (p.His983Asp) rs199475989
NM_032206.4(NLRC5):c.296-29A>C rs199475966
NM_032206.4(NLRC5):c.3113+100G>A rs199476300
NM_032206.4(NLRC5):c.3203+100G>C rs199475990
NM_032206.4(NLRC5):c.3248+56T>A rs199475991
NM_032206.4(NLRC5):c.3338+50C>T rs199475992
NM_032206.4(NLRC5):c.3338+59G>A rs199475993
NM_032206.4(NLRC5):c.3339-404C>T rs199475994
NM_032206.4(NLRC5):c.3506+149T>C rs199475996
NM_032206.4(NLRC5):c.3506+168G>A rs199475997
NM_032206.4(NLRC5):c.3506+7C>T rs199475995
NM_032206.4(NLRC5):c.3507-51C>T rs199475998
NM_032206.4(NLRC5):c.356-122C>T rs199475967
NM_032206.4(NLRC5):c.356-88G>A rs199475968
NM_032206.4(NLRC5):c.3596+42T>A rs199475999
NM_032206.4(NLRC5):c.3905G>A (p.Arg1302Gln) rs199476000
NM_032206.4(NLRC5):c.3920+20C>T rs199476001
NM_032206.4(NLRC5):c.3987-248C>T rs199476002
NM_032206.4(NLRC5):c.4018G>A (p.Val1340Met) rs199476003
NM_032206.4(NLRC5):c.4070+43G>A rs199476004
NM_032206.4(NLRC5):c.4154+23C>T rs199476005
NM_032206.4(NLRC5):c.424+238C>T rs199475970
NM_032206.4(NLRC5):c.424+276C>T rs199475971
NM_032206.4(NLRC5):c.424+46C>G rs199475969
NM_032206.4(NLRC5):c.4322+98A>G rs199476006
NM_032206.4(NLRC5):c.4365C>T (p.Val1455=) rs199476007
NM_032206.4(NLRC5):c.4407-9C>A rs199476008
NM_032206.4(NLRC5):c.4500-121G>A rs199476009
NM_032206.4(NLRC5):c.4584-134G>A rs199476010
NM_032206.4(NLRC5):c.4752-73G>A rs199476011
NM_032206.4(NLRC5):c.4835+61C>A rs199476012
NM_032206.4(NLRC5):c.4919+131G>A rs199476013
NM_032206.4(NLRC5):c.4920-60G>A rs199476014
NM_032206.4(NLRC5):c.5004-59G>C rs199476015
NM_032206.4(NLRC5):c.5172G>A (p.Ala1724=) rs199476016
NM_032206.4(NLRC5):c.5237+51G>A rs199476017
NM_032206.4(NLRC5):c.5238-50C>T rs199476018
NM_032206.4(NLRC5):c.5251A>G (p.Lys1751Glu) rs199476019
NM_032206.4(NLRC5):c.5321+11G>A rs199476020
NM_032206.4(NLRC5):c.5405+140G>A rs199476021
NM_032206.4(NLRC5):c.5474G>A (p.Ser1825Asn) rs199476022
NM_032206.4(NLRC5):c.847A>G (p.Ser283Gly) rs199475972
NM_032206.4(NLRC5):c.856T>G (p.Ser286Ala) rs1555520385

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.