ClinVar Miner

List of variants reported as uncertain significance for Methylmalonic acidemia with homocystinuria cblD by Illumina Clinical Services Laboratory,Illumina

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Total variants: 22
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HGVS dbSNP
NM_015702.3(MMADHC):c.*241A>G rs528409808
NM_015702.3(MMADHC):c.*267T>C rs546054980
NM_015702.3(MMADHC):c.-136G>C
NM_015702.3(MMADHC):c.-16A>G rs144111552
NM_015702.3(MMADHC):c.-52-3C>G rs886054922
NM_015702.3(MMADHC):c.-60G>A rs886054923
NM_015702.3(MMADHC):c.-62G>A rs886054924
NM_015702.3(MMADHC):c.10-3T>C rs886054921
NM_015702.3(MMADHC):c.166G>A (p.Val56Met)
NM_015702.3(MMADHC):c.244T>G (p.Cys82Gly) rs760590651
NM_015702.3(MMADHC):c.254A>G (p.Asn85Ser) rs767542742
NM_015702.3(MMADHC):c.373G>C (p.Gly125Arg)
NM_015702.3(MMADHC):c.515A>C (p.Lys172Thr) rs147318949
NM_015702.3(MMADHC):c.578T>C (p.Val193Ala) rs147370143
NM_015702.3(MMADHC):c.646C>G (p.Arg216Gly) rs141093638
NM_015702.3(MMADHC):c.696+13C>A
NM_015702.3(MMADHC):c.697-3C>T
NM_015702.3(MMADHC):c.699T>C (p.Phe233=)
NM_015702.3(MMADHC):c.735T>G (p.Thr245=) rs530553915
NM_015702.3(MMADHC):c.73G>T (p.Val25Phe)
NM_015702.3(MMADHC):c.759A>T (p.Gly253=) rs886054920
NM_015702.3(MMADHC):c.800A>G (p.His267Arg) rs753424109

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