ClinVar Miner

List of variants in gene MOCS1 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001358530.2(MOCS1):c.124-216A>G rs3008822 0.50249
NM_001358530.2(MOCS1):c.*824C>G rs11968491 0.06790
NM_001358530.2(MOCS1):c.583+10T>A rs34757428 0.06768
NM_001358530.2(MOCS1):c.716T>A (p.Leu239His) rs7762875 0.06302
NM_001358530.2(MOCS1):c.*451C>T rs41273136 0.06093
NM_001358530.2(MOCS1):c.*1334A>C rs3749999 0.05702
NM_001358530.2(MOCS1):c.698C>T (p.Ala233Val) rs35825585 0.05422
NM_001358530.2(MOCS1):c.*987C>T rs7758412 0.04471
NM_001358530.2(MOCS1):c.*378G>A rs11968529 0.04433
NM_001358530.2(MOCS1):c.1800C>T (p.Ala600=) rs41273138 0.03810
NM_001358530.2(MOCS1):c.1169C>A (p.Pro390His) rs11969769 0.03639
NM_001358530.2(MOCS1):c.583+6C>T rs111409017 0.03125
NM_001358530.2(MOCS1):c.330C>T (p.Leu110=) rs61746375 0.02544
NM_001358530.2(MOCS1):c.*734C>G rs1063171 0.02273
NM_001358530.2(MOCS1):c.645+9G>C rs73732319 0.02256
NM_001358530.2(MOCS1):c.1316G>A (p.Arg439Gln) rs41273142 0.02099
NM_001358530.2(MOCS1):c.1715G>A (p.Arg572His) rs41273140 0.01571
NM_001358530.2(MOCS1):c.*1136A>C rs60326448 0.01180
NM_001358530.2(MOCS1):c.*1002C>T rs115706925 0.01175
NM_001358530.2(MOCS1):c.*578C>T rs147395035 0.00739
NM_001358530.2(MOCS1):c.*1405G>C rs3749998 0.00676
NM_001358530.2(MOCS1):c.*1113T>G rs3828937 0.00672
NM_001358530.2(MOCS1):c.1212G>C (p.Pro404=) rs11969233
NM_001358530.2(MOCS1):c.1355G>T (p.Arg452Leu) rs11969206

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.