ClinVar Miner

List of variants reported as uncertain significance for Multiple endocrine neoplasia, type 1 by Illumina Clinical Services Laboratory,Illumina

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Total variants: 22
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HGVS dbSNP
NM_000244.3(MEN1):c.*104C>T rs886048477
NM_000244.3(MEN1):c.*272T>C rs563783609
NM_000244.3(MEN1):c.*373G>C rs886048476
NM_000244.3(MEN1):c.*392G>A rs886048475
NM_000244.3(MEN1):c.*438C>T rs886048474
NM_000244.3(MEN1):c.*89G>A rs886048478
NM_000244.3(MEN1):c.-94G>A rs886048480
NM_000244.3(MEN1):c.1201-10C>T rs762303621
NM_000244.3(MEN1):c.327A>C (p.Glu109Asp) rs773976527
NM_000244.3(MEN1):c.585G>A (p.Gly195=) rs547249181
NM_000244.3(MEN1):c.956G>A (p.Arg319Gln) rs771645621
NM_001370259.2(MEN1):c.*245C>T
NM_001370259.2(MEN1):c.*341C>G
NM_001370259.2(MEN1):c.*400G>A
NM_001370259.2(MEN1):c.*470A>G rs778272737
NM_001370259.2(MEN1):c.*693T>C
NM_001370259.2(MEN1):c.1414G>C (p.Gly472Arg)
NM_001370259.2(MEN1):c.1618C>T (p.Pro540Ser) rs745404679
NM_001370259.2(MEN1):c.274C>A (p.Arg92Ser)
NM_001370259.2(MEN1):c.655-6C>G rs77461664
NM_001370259.2(MEN1):c.849G>T (p.Leu283=)
NM_001370259.2(MEN1):c.965T>C (p.Met322Thr)

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