ClinVar Miner

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

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Gene type:
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Total variants: 27
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HGVS dbSNP gnomAD frequency
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.681-37C>T rs191998453 0.00215
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.1608C>T (p.Ile536=) rs542779722 0.00002
NM_002880.4(RAF1):c.639T>C (p.Thr213=) rs397516823 0.00002
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.1203G>A (p.Arg401=)
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.1917G>A (p.Leu639=)
NM_002880.4(RAF1):c.424-10C>G
NM_002880.4(RAF1):c.594T>C (p.Asn198=)
NM_002880.4(RAF1):c.680+11A>G rs868108376

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