ClinVar Miner

List of variants in gene RIMS1 reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
Download table as spreadsheet
HGVS dbSNP
NC_000006.11:g.72892536T>C
NM_001168407.2(RIMS1):c.1625+8366G>C
NM_001168407.2(RIMS1):c.1625+8372G>A rs374938269
NM_001168407.2(RIMS1):c.794+27del
NM_001168407.2(RIMS1):c.794+27dup
NM_001168409.2(RIMS1):c.-58A>G rs192179523
NM_014989.5(RIMS1):c.1083A>G (p.Leu361=) rs2463730
NM_014989.5(RIMS1):c.1209G>A (p.Ala403=) rs114505309
NM_014989.5(RIMS1):c.1459G>A (p.Ala487Thr) rs200422266
NM_014989.5(RIMS1):c.1533G>A (p.Pro511=) rs201473375
NM_014989.5(RIMS1):c.165-5C>G rs532652925
NM_014989.5(RIMS1):c.1776G>A (p.Glu592=) rs77121218
NM_014989.5(RIMS1):c.2082-9T>C rs199746605
NM_014989.5(RIMS1):c.2670T>C (p.His890=) rs34821160
NM_014989.5(RIMS1):c.2699-8T>C rs149883454
NM_014989.5(RIMS1):c.2895G>A (p.Pro965=) rs41265493
NM_014989.5(RIMS1):c.3171C>T (p.Ser1057=) rs201355521
NM_014989.5(RIMS1):c.3194+9C>A rs564292772
NM_014989.5(RIMS1):c.3308+12T>G
NM_014989.5(RIMS1):c.3399-4A>G rs368216570
NM_014989.5(RIMS1):c.3470C>T (p.Pro1157Leu) rs41265501
NM_014989.5(RIMS1):c.3941T>C (p.Leu1314Pro) rs201798320
NM_014989.5(RIMS1):c.438C>T (p.Arg146=) rs142196418
NM_014989.5(RIMS1):c.4505+10G>A rs202016391
NM_014989.5(RIMS1):c.4506-5G>A rs201556693
NM_014989.5(RIMS1):c.4548C>T (p.Phe1516=) rs2815738
NM_014989.5(RIMS1):c.458A>C (p.Asn153Thr)
NM_014989.5(RIMS1):c.459+12A>G
NM_014989.5(RIMS1):c.4618+20del rs113359739
NM_014989.5(RIMS1):c.4618+20dup rs113359739
NM_014989.5(RIMS1):c.4842A>G (p.Pro1614=) rs376289027
NM_014989.5(RIMS1):c.4860+15G>A rs553488575
NM_014989.5(RIMS1):c.4923C>T (p.Ile1641=) rs144188801
NM_014989.5(RIMS1):c.4983G>A (p.Pro1661=) rs377743730
NM_014989.5(RIMS1):c.5076A>G (p.Ser1692=) rs61736795
NM_014989.5(RIMS1):c.594A>G (p.Thr198=) rs149442461
NM_014989.5(RIMS1):c.648G>A (p.Ser216=) rs116303981
NM_014989.5(RIMS1):c.666A>G (p.Leu222=) rs2249021
NM_014989.5(RIMS1):c.743C>T (p.Ser248Leu) rs116476753
NM_014989.5(RIMS1):c.813-14T>G rs180682682
NM_014989.5(RIMS1):c.942G>A (p.Arg314=) rs185069362

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.