ClinVar Miner

List of variants studied for Congenital disorder of glycosylation type 1M by OMIM

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Total variants: 6

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HGVS	dbSNP
NM_014908.3(DOLK):c.1222C>G (p.His408Asp)	rs387907030
NM_014908.3(DOLK):c.1322A>C (p.Tyr441Ser)	rs137853110
NM_014908.3(DOLK):c.295T>A (p.Cys99Ser)	rs137853109
NM_014908.3(DOLK):c.2T>C (p.Met1Thr)	rs587777137
NM_014908.3(DOLK):c.3G>A (p.Met1Ile)	rs1564546510
NM_014908.3(DOLK):c.912G>T (p.Trp304Cys)	rs1564545929

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