ClinVar Miner

List of variants in gene EIF4G1 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_198241.3(EIF4G1):c.4383C>T (p.Phe1461=) rs111921843 0.00983
NM_198241.3(EIF4G1):c.4551C>T (p.Asp1517=) rs11559218 0.00509
NM_198241.3(EIF4G1):c.2976A>G (p.Pro992=) rs112420733 0.00332
NM_198241.3(EIF4G1):c.1796-3C>T rs190378563 0.00193
NM_198241.3(EIF4G1):c.2609A>C (p.Glu870Ala) rs375514524 0.00002
NM_198241.3(EIF4G1):c.1673C>T (p.Ser558Phe) rs1241165074 0.00001
NM_198241.3(EIF4G1):c.1147C>T (p.Pro383Ser)
NM_198241.3(EIF4G1):c.2416A>G (p.Ile806Val)
NM_198241.3(EIF4G1):c.3387G>T (p.Ala1129=)
NM_198241.3(EIF4G1):c.3648T>C (p.Arg1216=)
NM_198241.3(EIF4G1):c.3685C>G (p.Pro1229Ala) rs35629949
NM_198241.3(EIF4G1):c.4464T>C (p.Tyr1488=)

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.