New variants, new classification

New variant:
c.1390C>A; p.(Gln464Lys); NM_000540.3(RYR1):c.5132A>G p.(Gln464Lys)
EMHG pathogenic, VCEP: likely pathogenic

Updated variant:
c.7060G>A; p.(Val2354Met): EMHG changed from VUS to pathogenic
c.7292A>T; p.(Asp2431Val): EMHG changed from VUS to pathogenic
c.7879G>C; p.(Val2627Leu): EMHG changed from VUS to pathogenic
c.8189A>G; p.(Asp2730Gly): EMHG changed from VUS to likely pathogenic
c.14918C>T; p.(Pro4973Leu): EMHG changed from likely pathogenic to pathogenic