ClinVar Miner

List of variants reported as uncertain significance for Multiple endocrine neoplasia, type 4 by Illumina Clinical Services Laboratory,Illumina

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Total variants: 33
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HGVS dbSNP
NM_004064.4(CDKN1B):c.*1073C>T rs751656637
NM_004064.4(CDKN1B):c.*1186T>C rs886049087
NM_004064.4(CDKN1B):c.*204T>C rs886049083
NM_004064.4(CDKN1B):c.*379T>C rs773825212
NM_004064.4(CDKN1B):c.*421A>G rs749773766
NM_004064.4(CDKN1B):c.*452C>T rs762469235
NM_004064.4(CDKN1B):c.*746G>T rs886049085
NM_004064.4(CDKN1B):c.*88A>G rs886049082
NM_004064.4(CDKN1B):c.*935C>T rs778375300
NM_004064.4(CDKN1B):c.*948T>C rs886049086
NM_004064.4(CDKN1B):c.*980G>A rs756925371
NM_004064.4(CDKN1B):c.-336A>G rs886049080
NM_004064.4(CDKN1B):c.-366C>T rs886049079
NM_004064.4(CDKN1B):c.-371C>T rs11550615
NM_004064.4(CDKN1B):c.-386C>T rs886049078
NM_004064.4(CDKN1B):c.-471T>G rs886049077
NM_004064.4(CDKN1B):c.279G>A (p.Arg93=) rs766901538
NM_004064.4(CDKN1B):c.520G>A (p.Val174Ile) rs766659283
NM_004064.5(CDKN1B):c.*1024G>C
NM_004064.5(CDKN1B):c.*1223A>C
NM_004064.5(CDKN1B):c.*437A>G
NM_004064.5(CDKN1B):c.*815C>T
NM_004064.5(CDKN1B):c.*831A>C
NM_004064.5(CDKN1B):c.*844C>G
NM_004064.5(CDKN1B):c.*92A>G
NM_004064.5(CDKN1B):c.*973G>T
NM_004064.5(CDKN1B):c.-222C>T
NM_004064.5(CDKN1B):c.-226C>T
NM_004064.5(CDKN1B):c.-374G>A
NM_004064.5(CDKN1B):c.-386C>G
NM_004064.5(CDKN1B):c.-423G>A
NM_004064.5(CDKN1B):c.-73G>A rs1592280605
NM_004064.5(CDKN1B):c.-7G>C rs751341214

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