ClinVar Miner

Submissions for variant NM_006182.4(DDR2):c.757G>T (p.Gly253Cys)

dbSNP: rs376303676
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000421258 SCV000505163 likely pathogenic Squamous cell lung carcinoma 2014-12-26 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000441392 SCV000505720 not provided Non-small cell lung carcinoma 2016-03-10 no assertion provided literature only

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