ClinVar Miner

Submissions for variant NM_182925.5(FLT4):c.2104G>T (p.Ala702Ser)

gnomAD frequency: 0.00003 dbSNP: rs746659265

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Mendelics	RCV000987647	SCV001137045	uncertain significance	Carcinoma of colon	2019-05-28	criteria provided, single submitter	clinical testing

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