List of variants in gene RAF1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.*190G>A	rs528863135	0.00335
NM_002880.4(RAF1):c.*110T>C	rs550188508	0.00112
NM_002880.4(RAF1):c.1830A>G (p.Gln610=)	rs141791080	0.00088
NM_002880.4(RAF1):c.-201C>A	rs532668125	0.00073
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.576A>G (p.Gln192=)	rs148759910	0.00016
NM_002880.4(RAF1):c.94A>G (p.Ile32Val)	rs372738063	0.00013
NM_002880.4(RAF1):c.934G>A (p.Val312Met)	rs555034652	0.00002
NM_002880.4(RAF1):c.710_737dup
NM_002880.4(RAF1):c.-204G>C	rs547543588
NM_002880.4(RAF1):c.1629G>A (p.Thr543=)	rs5746244
NM_002880.4(RAF1):c.60C>T (p.Ala20=)	rs755869970
NM_002880.4(RAF1):c.835-1599G>T
NM_002880.4(RAF1):c.835-225T>G
NM_002880.4(RAF1):c.835-362C>T
NM_002880.4(RAF1):c.835-505C>G

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