ClinVar Miner

List of variants in gene RAF1 reported as benign for Noonan syndrome and Noonan-related syndrome

Included ClinVar conditions (50):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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NM_002880.3(RAF1):c.1108+9_1108+21del rs727504451
NM_002880.3(RAF1):c.1141G>A (p.Asp381Asn) rs559632360
NM_002880.3(RAF1):c.119G>A (p.Arg40His) rs192632236
NM_002880.3(RAF1):c.1587G>A (p.Ser529=) rs114687276
NM_002880.3(RAF1):c.1629G>A (p.Thr543=) rs5746244
NM_002880.3(RAF1):c.1629G>C (p.Thr543=) rs5746244
NM_002880.3(RAF1):c.1668+4A>G rs771344560
NM_002880.3(RAF1):c.1755A>G (p.Val585=) rs3730296
NM_002880.3(RAF1):c.1830A>G (p.Gln610=) rs141791080
NM_002880.3(RAF1):c.1914G>A (p.Thr638=) rs144876026
NM_002880.3(RAF1):c.1941C>T (p.Val647=) rs3730297
NM_002880.3(RAF1):c.212A>G (p.Asn71Ser) rs184022679
NM_002880.3(RAF1):c.923C>T (p.Pro308Leu) rs5746220
NM_002880.3(RAF1):c.94A>G (p.Ile32Val) rs372738063

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