ClinVar Miner

List of variants in gene RIPK4 reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 120
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020639.3(RIPK4):c.1996A>G (p.Met666Val) rs3746891 0.98229
NM_020639.3(RIPK4):c.*90T>C rs6586232 0.79267
NM_020639.3(RIPK4):c.1548C>T (p.Asp516=) rs2838113 0.53199
NM_020639.3(RIPK4):c.2331G>A (p.Thr777=) rs7276592 0.41978
NM_020639.3(RIPK4):c.1476G>A (p.Ala492=) rs3746893 0.41949
NM_020639.3(RIPK4):c.1203C>T (p.Gly401=) rs3746894 0.41922
NM_020639.3(RIPK4):c.*560A>G rs3746890 0.41259
NM_020639.3(RIPK4):c.*782_*783dup rs34075882 0.40146
NM_020639.3(RIPK4):c.1005G>T (p.Leu335=) rs2277789 0.38050
NM_020639.3(RIPK4):c.*983G>A rs3171532 0.36576
NM_020639.3(RIPK4):c.35C>G (p.Ala12Gly) rs6586239 0.15988
NM_020639.3(RIPK4):c.159G>A (p.Ser53=) rs6586238 0.14219
NM_020639.3(RIPK4):c.360A>C (p.Arg120=) rs13049286 0.13916
NM_020639.3(RIPK4):c.327T>C (p.Ala109=) rs2277791 0.13904
NM_020639.3(RIPK4):c.*275T>C rs73369674 0.05243
NM_020639.3(RIPK4):c.*748A>G rs17113877 0.02775
NM_020639.3(RIPK4):c.*219T>G rs112292749 0.02518
NM_020639.3(RIPK4):c.*578C>A rs17113879 0.02132
NM_020639.3(RIPK4):c.*741G>A rs13050509 0.01754
NM_020639.3(RIPK4):c.1587G>A (p.Ser529=) rs61740546 0.01687
NM_020639.3(RIPK4):c.1425G>A (p.Leu475=) rs56092943 0.01339
NM_020639.3(RIPK4):c.117G>A (p.Val39=) rs147023104 0.01319
NM_020639.3(RIPK4):c.7G>A (p.Gly3Ser) rs199825512 0.01162
NM_020639.3(RIPK4):c.1311C>T (p.Ser437=) rs56149248 0.01122
NM_020639.3(RIPK4):c.1119G>T (p.Gly373=) rs61744790 0.01056
NM_020639.3(RIPK4):c.*707G>A rs115461340 0.01049
NM_020639.3(RIPK4):c.*550C>G rs113816274 0.00795
NM_020639.3(RIPK4):c.2101C>T (p.Pro701Ser) rs35537517 0.00597
NM_020639.3(RIPK4):c.*715A>G rs77257940 0.00513
NM_020639.3(RIPK4):c.1884C>T (p.Ser628=) rs55812846 0.00492
NM_020639.3(RIPK4):c.*1025G>T rs73216989 0.00478
NM_020639.3(RIPK4):c.1617G>A (p.Thr539=) rs61740535 0.00411
NM_020639.3(RIPK4):c.*747T>A rs188837957 0.00375
NM_020639.3(RIPK4):c.1941G>A (p.Thr647=) rs116160025 0.00314
NM_020639.3(RIPK4):c.819G>A (p.Arg273=) rs139503982 0.00290
NM_020639.3(RIPK4):c.*416C>T rs187507566 0.00280
NM_020639.3(RIPK4):c.*1234G>A rs115885677 0.00180
NM_020639.3(RIPK4):c.*73G>A rs188084540 0.00178
NM_020639.3(RIPK4):c.*637G>A rs572218247 0.00137
NM_020639.3(RIPK4):c.267C>T (p.Arg89=) rs55798804 0.00131
NM_020639.3(RIPK4):c.*701A>G rs553704130 0.00130
NM_020639.3(RIPK4):c.832+2T>C rs146341788 0.00129
NM_020639.3(RIPK4):c.303G>A (p.Thr101=) rs2277792 0.00088
NM_020639.3(RIPK4):c.2008G>A (p.Gly670Ser) rs148192173 0.00081
NM_020639.3(RIPK4):c.1243G>A (p.Val415Met) rs55645753 0.00073
NM_020639.3(RIPK4):c.*978C>G rs76434022 0.00069
NM_020639.3(RIPK4):c.*1361T>A rs190283912 0.00061
NM_020639.3(RIPK4):c.252G>A (p.Val84=) rs138268998 0.00052
NM_020639.3(RIPK4):c.2145C>T (p.His715=) rs61739694 0.00041
NM_020639.3(RIPK4):c.2277C>T (p.Ala759=) rs201802815 0.00041
NM_020639.3(RIPK4):c.2323G>A (p.Ala775Thr) rs142879262 0.00038
NM_020639.3(RIPK4):c.936+6G>A rs199827829 0.00035
NM_020639.3(RIPK4):c.812G>A (p.Arg271Gln) rs144179743 0.00030
NM_020639.3(RIPK4):c.1039G>A (p.Val347Ile) rs150480670 0.00024
NM_020639.3(RIPK4):c.*204G>A rs533596469 0.00023
NM_020639.3(RIPK4):c.2250G>A (p.Thr750=) rs201024640 0.00023
NM_020639.3(RIPK4):c.*59C>T rs886057088 0.00019
NM_020639.3(RIPK4):c.2325C>T (p.Ala775=) rs148947402 0.00014
NM_020639.3(RIPK4):c.*1203A>T rs555235524 0.00013
NM_020639.3(RIPK4):c.277G>A (p.Gly93Ser) rs372343704 0.00013
NM_020639.3(RIPK4):c.1779G>A (p.Pro593=) rs202049606 0.00011
NM_020639.3(RIPK4):c.2041G>A (p.Gly681Arg) rs371444612 0.00011
NM_020639.3(RIPK4):c.*1248C>T rs755144689 0.00010
NM_020639.3(RIPK4):c.*60G>A rs886057087 0.00010
NM_020639.3(RIPK4):c.*1117T>C rs941229311 0.00009
NM_020639.3(RIPK4):c.1100G>T (p.Ser367Ile) rs201477363 0.00009
NM_020639.3(RIPK4):c.1862G>A (p.Arg621His) rs56056485 0.00009
NM_020639.3(RIPK4):c.959G>A (p.Arg320Gln) rs187728866 0.00009
NM_020639.3(RIPK4):c.1980C>T (p.Gly660=) rs144946647 0.00008
NM_020639.3(RIPK4):c.2296C>G (p.Leu766Val) rs200025631 0.00008
NM_020639.3(RIPK4):c.*1081C>T rs886057082 0.00006
NM_020639.3(RIPK4):c.*281G>A rs576215477 0.00006
NM_020639.3(RIPK4):c.1344C>T (p.Ala448=) rs577583084 0.00006
NM_020639.3(RIPK4):c.474+14C>T rs532592992 0.00006
NM_020639.3(RIPK4):c.*1206A>G rs369347545 0.00005
NM_020639.3(RIPK4):c.2139C>T (p.His713=) rs202070628 0.00005
NM_020639.3(RIPK4):c.504C>T (p.Asn168=) rs200523041 0.00005
NM_020639.3(RIPK4):c.*823A>G rs182698444 0.00004
NM_020639.3(RIPK4):c.1137C>T (p.Ser379=) rs200420912 0.00004
NM_020639.3(RIPK4):c.1164G>A (p.Ser388=) rs535635195 0.00004
NM_020639.3(RIPK4):c.1561C>T (p.Arg521Trp) rs148559295 0.00003
NM_020639.3(RIPK4):c.*1447A>C rs1356634807 0.00002
NM_020639.3(RIPK4):c.1195+8G>C rs750525932 0.00002
NM_020639.3(RIPK4):c.1453G>A (p.Gly485Ser) rs376154775 0.00002
NM_020639.3(RIPK4):c.1530T>C (p.Phe510=) rs761959722 0.00002
NM_020639.3(RIPK4):c.1995C>T (p.Ala665=) rs758168721 0.00002
NM_020639.3(RIPK4):c.302C>T (p.Thr101Met) rs778210206 0.00002
NM_020639.3(RIPK4):c.779G>A (p.Arg260His) rs549925444 0.00002
NM_020639.2(RIPK4):c.-44C>G rs774016517 0.00001
NM_020639.3(RIPK4):c.*1376C>T rs938071196 0.00001
NM_020639.3(RIPK4):c.*142G>A rs886057086 0.00001
NM_020639.3(RIPK4):c.*298A>G rs1325503303 0.00001
NM_020639.3(RIPK4):c.*729C>T rs886057084 0.00001
NM_020639.3(RIPK4):c.*72C>T rs1193530619 0.00001
NM_020639.3(RIPK4):c.*824C>T rs1413927849 0.00001
NM_020639.3(RIPK4):c.1106A>G (p.Lys369Arg) rs377595424 0.00001
NM_020639.3(RIPK4):c.1477C>T (p.Arg493Trp) rs745574177 0.00001
NM_020639.3(RIPK4):c.2001C>G (p.Thr667=) rs759122850 0.00001
NM_020639.3(RIPK4):c.271C>A (p.Pro91Thr) rs886057089 0.00001
NM_020639.3(RIPK4):c.377C>T (p.Ala126Val) rs773242499 0.00001
NM_020639.3(RIPK4):c.899A>T (p.Asp300Val) rs1479686520 0.00001
NM_020639.3(RIPK4):c.*1039dup rs886057083
NM_020639.3(RIPK4):c.*1151G>A rs948234291
NM_020639.3(RIPK4):c.*1172T>C rs2061146329
NM_020639.3(RIPK4):c.*1192A>G rs543933391
NM_020639.3(RIPK4):c.*1420T>G rs1194984878
NM_020639.3(RIPK4):c.*161G>A rs536240693
NM_020639.3(RIPK4):c.*173C>T rs1008340022
NM_020639.3(RIPK4):c.*201C>T rs886057085
NM_020639.3(RIPK4):c.*215G>C rs115041500
NM_020639.3(RIPK4):c.*215G>T rs115041500
NM_020639.3(RIPK4):c.*273A>C rs1052236618
NM_020639.3(RIPK4):c.*961G>A rs1601672028
NM_020639.3(RIPK4):c.1079C>T (p.Ser360Phe) rs1470223809
NM_020639.3(RIPK4):c.1193G>T (p.Ser398Ile) rs201219158
NM_020639.3(RIPK4):c.1694T>G (p.Leu565Arg) rs2061153760
NM_020639.3(RIPK4):c.59G>A (p.Gly20Asp) rs2061239545
NM_020639.3(RIPK4):c.630G>A (p.Ala210=) rs2838114
NM_020639.3(RIPK4):c.630G>C (p.Ala210=) rs2838114
NM_020639.3(RIPK4):c.755C>T (p.Pro252Leu) rs770860869

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.