ClinVar Miner

Submissions for variant NM_002755.3(MAP2K1):c.171G>T (p.Lys57Asn) (rs869025608)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000208748 SCV000264640 pathogenic Cardio-facio-cutaneous syndrome 2016-03-03 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438528 SCV000504534 likely pathogenic Cutaneous melanoma 2014-12-26 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421288 SCV000504535 pathogenic Non-small cell lung cancer 2014-10-02 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000428485 SCV000504536 likely pathogenic Lung adenocarcinoma 2015-07-14 no assertion criteria provided literature only

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