ClinVar Miner

List of variants in gene RAF1 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_002880.4(RAF1):c.1830A>G (p.Gln610=) rs141791080 0.00088
NM_002880.4(RAF1):c.-59C>A rs201603517 0.00032
NM_002880.4(RAF1):c.909A>C (p.Thr303=) rs5746219 0.00025
NM_002880.4(RAF1):c.122G>A (p.Arg41Gln) rs145611571 0.00016
NM_002880.4(RAF1):c.576A>G (p.Gln192=) rs148759910 0.00016
NM_002880.4(RAF1):c.680+6T>C rs371846795 0.00014
NM_002880.4(RAF1):c.94A>G (p.Ile32Val) rs372738063 0.00013
NM_002880.4(RAF1):c.1515T>C (p.Pro505=) rs140668986 0.00007
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.1108+15C>T rs727503383 0.00003
NM_002880.4(RAF1):c.63G>A (p.Val21=) rs377377296 0.00003
NM_002880.4(RAF1):c.639T>C (p.Thr213=) rs397516823 0.00002
NM_002880.3(RAF1):c.-382A>G rs397516812 0.00001
NM_002880.4(RAF1):c.-169G>A rs727504398 0.00001
NM_002880.4(RAF1):c.171T>C (p.Thr57=) rs751571550 0.00001
NM_002880.4(RAF1):c.708C>T (p.His236=) rs370658857 0.00001
NM_002880.4(RAF1):c.990+9A>G rs559532794 0.00001
NM_002880.3(RAF1):c.-340_-339GA[1] rs527774250
NM_002880.4(RAF1):c.-204G>C rs547543588
NM_002880.4(RAF1):c.-267G>A rs116247741
NM_002880.4(RAF1):c.-298C>T rs727504387
NM_002880.4(RAF1):c.1108+9_1108+21del rs727504451
NM_002880.4(RAF1):c.1314C>T (p.Thr438=) rs147547744
NM_002880.4(RAF1):c.1695T>C (p.Tyr565=) rs397516817
NM_002880.4(RAF1):c.276A>G (p.Gln92=) rs876657568
NM_002880.4(RAF1):c.834+8G>A rs727504615
NM_002880.4(RAF1):c.876C>T (p.Ala292=) rs397516831

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