ClinVar Miner

List of variants in gene BRAF reported as uncertain significance for Noonan syndrome with multiple lentigines

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Total variants: 8
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HGVS dbSNP
NM_004333.4(BRAF):c.2128-16_2128-15delCT rs886062015
NM_004333.5(BRAF):c.2128-28dup rs60814637
NM_004333.6(BRAF):c.*3C>T rs746680490
NM_004333.6(BRAF):c.*7T>C rs727502903
NM_004333.6(BRAF):c.2128-15dup rs373442098
NM_004333.6(BRAF):c.2128-27_2128-16delinsTCT rs886062016
NM_004333.6(BRAF):c.2128-4del rs886062014
NM_004333.6(BRAF):c.981-14C>A rs200002171

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