Related gene-specific medical variations for Gene (Select 10544) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3310280	NM_006404.5(PROCR):c.26T>C (p.Leu9Pro)	MMP24-AS1-EDEM2, PROCR (L9P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310279	NM_006404.5(PROCR):c.305A>G (p.Gln102Arg)	MMP24-AS1-EDEM2, PROCR (Q102R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2533397	NM_006404.5(PROCR):c.554C>A (p.Thr185Asn)	MMP24-AS1-EDEM2, PROCR (T185N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467830	NM_006404.5(PROCR):c.383A>T (p.His128Leu)	MMP24-AS1-EDEM2, PROCR (H128L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411277	NM_006404.5(PROCR):c.629C>T (p.Ser210Leu)	MMP24-AS1-EDEM2, PROCR (S210L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400339	NM_006404.5(PROCR):c.517C>G (p.Arg173Gly)	MMP24-AS1-EDEM2, PROCR (R173G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366201	NM_006404.5(PROCR):c.164C>T (p.Thr55Met)	MMP24-AS1-EDEM2, PROCR (T55M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317503	NM_006404.5(PROCR):c.536G>A (p.Arg179Gln)	MMP24-AS1-EDEM2, PROCR (R179Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2301038	NM_006404.5(PROCR):c.283G>T (p.Gly95Cys)	MMP24-AS1-EDEM2, PROCR (G95C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210619	NM_006404.5(PROCR):c.311G>C (p.Arg104Pro)	MMP24-AS1-EDEM2, PROCR (R104P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 737408	NM_006404.5(PROCR):c.393C>T (p.Phe131=)	MMP24-AS1-EDEM2, PROCR	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 731572	NM_006404.5(PROCR):c.262T>C (p.Ser88Pro)	MMP24-AS1-EDEM2, PROCR (S88P)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign