List of variants reported as uncertain significance for Methylcobalamin deficiency type cblG by Revvity Omics, Revvity

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000254.3(MTR):c.1862A>G (p.Asp621Gly)	rs61736440	0.00081
NM_000254.3(MTR):c.1141G>A (p.Ala381Thr)	rs144777709	0.00073
NM_000254.3(MTR):c.2813G>T (p.Ser938Ile)	rs774910076	0.00002
NM_000254.3(MTR):c.2032G>T (p.Ala678Ser)	rs759130222	0.00001
NM_000254.3(MTR):c.128_129delinsTT (p.Arg43Leu)	rs1660806761
NM_000254.3(MTR):c.3718G>T (p.Asp1240Tyr)

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