ClinVar Miner

Submissions for variant NM_000092.4(COL4A4):c.3829C>T (p.Pro1277Ser) (rs1037084154)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare	RCV000625552	SCV000746047	uncertain significance	Alport syndrome 3, autosomal dominant	2017-09-18	no assertion criteria provided	clinical testing

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