ClinVar Miner

List of variants in gene RAF1 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002880.4(RAF1):c.1755A>G (p.Val585=) rs3730296 0.02125
NM_002880.4(RAF1):c.1193+39T>C rs2290161 0.01394
NM_002880.4(RAF1):c.991-42T>C rs5746226 0.00943
NM_002880.4(RAF1):c.991-43T>C rs5746225 0.00943
NM_002880.4(RAF1):c.1669-13T>C rs147475396 0.00819
NM_002880.4(RAF1):c.681-37C>T rs191998453 0.00215
NM_002880.4(RAF1):c.1830A>G (p.Gln610=) rs141791080 0.00088
NM_002880.4(RAF1):c.212A>G (p.Asn71Ser) rs184022679 0.00029
NM_002880.4(RAF1):c.909A>C (p.Thr303=) rs5746219 0.00025
NM_002880.4(RAF1):c.124G>A (p.Ala42Thr) rs200856000 0.00021
NM_002880.4(RAF1):c.125C>T (p.Ala42Val) rs11549992 0.00021
NM_002880.4(RAF1):c.122G>A (p.Arg41Gln) rs145611571 0.00016
NM_002880.4(RAF1):c.1721A>G (p.Tyr574Cys) rs370242565 0.00012
NM_002880.4(RAF1):c.66T>G (p.Phe22Leu) rs397516824 0.00006
NM_002880.4(RAF1):c.435G>A (p.Thr145=) rs371565419 0.00004
NM_002880.4(RAF1):c.863-16T>C rs770891566 0.00004
NM_002880.4(RAF1):c.1821G>A (p.Glu607=) rs747437834 0.00003
NM_002880.4(RAF1):c.53A>G (p.Lys18Arg) rs150944421 0.00003
NM_002880.4(RAF1):c.1608C>T (p.Ile536=) rs542779722 0.00002
NM_002880.4(RAF1):c.639T>C (p.Thr213=) rs397516823 0.00002
NM_002880.4(RAF1):c.1687C>T (p.Arg563Ter) rs532786413 0.00001
NM_002880.4(RAF1):c.1914G>A (p.Thr638=) rs144876026 0.00001
NM_002880.4(RAF1):c.513A>G (p.Lys171=) rs561163045 0.00001
NM_002880.4(RAF1):c.771G>A (p.Ser257=) rs764065991 0.00001
NM_002880.4(RAF1):c.907A>G (p.Thr303Ala) rs775898894 0.00001
NM_002880.3(RAF1):c.1804-11_1804-7dup rs727503382
NM_002880.4(RAF1):c.-262G>C
NM_002880.4(RAF1):c.1108+9_1108+21del rs727504451
NM_002880.4(RAF1):c.1148C>A (p.Thr383Asn)
NM_002880.4(RAF1):c.1203G>A (p.Arg401=)
NM_002880.4(RAF1):c.1309G>C (p.Glu437Gln)
NM_002880.4(RAF1):c.1336A>G (p.Ile446Val)
NM_002880.4(RAF1):c.1629G>C (p.Thr543=) rs5746244
NM_002880.4(RAF1):c.1668+10_1668+11del rs730880997
NM_002880.4(RAF1):c.1837C>G (p.Leu613Val) rs80338797
NM_002880.4(RAF1):c.1917G>A (p.Leu639=)
NM_002880.4(RAF1):c.310G>A (p.Glu104Lys)
NM_002880.4(RAF1):c.321-14dup rs202103447
NM_002880.4(RAF1):c.412A>G (p.Thr138Ala)
NM_002880.4(RAF1):c.424-10C>G
NM_002880.4(RAF1):c.438C>A (p.Phe146Leu) rs794727717
NM_002880.4(RAF1):c.594T>C (p.Asn198=)
NM_002880.4(RAF1):c.680+11A>G rs868108376
NM_002880.4(RAF1):c.68_70del (p.Asp23del) rs749549707
NM_002880.4(RAF1):c.781C>G (p.Pro261Ala) rs121434594
NM_002880.4(RAF1):c.828G>T (p.Met276Ile)
NM_002880.4(RAF1):c.834+611A>G
NM_002880.4(RAF1):c.834+614_834+618delinsTGTTAT
NM_002880.4(RAF1):c.834+646_834+647insCA
NM_002880.4(RAF1):c.841A>G (p.Ile281Val)
NM_002880.4(RAF1):c.869C>A (p.Pro290His) rs2058820862
NM_002880.4(RAF1):c.989T>C (p.Ile330Thr)

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.