List of variants in gene COL4A5 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_033380.3(COL4A5):c.1871G>A (p.Gly624Asp)	rs104886142	0.00005
NM_033380.3(COL4A5):c.2348C>T (p.Pro783Leu)	rs747288279	0.00005
NM_033380.3(COL4A5):c.2998G>A (p.Gly1000Arg)	rs2067110688	0.00003
NM_033380.3(COL4A5):c.5048G>A (p.Arg1683Gln)	rs104886308	0.00002
NM_033380.3(COL4A5):c.1276G>A (p.Gly426Arg)	rs104886111	0.00001
NM_033380.3(COL4A5):c.231+1G>A	rs104886349	0.00001
NM_033380.3(COL4A5):c.1807G>C (p.Gly603Arg)
NM_033380.3(COL4A5):c.1912G>C (p.Gly638Arg)
NM_033380.3(COL4A5):c.2482G>C (p.Gly828Arg)
NM_033380.3(COL4A5):c.3061_3062delinsAT (p.Gly1021Ile)
NM_033380.3(COL4A5):c.3731G>A (p.Gly1244Asp)	rs104886261
NM_033380.3(COL4A5):c.3785G>A (p.Arg1262Lys)
NM_033380.3(COL4A5):c.4964T>G (p.Leu1655Arg)	rs104886303
NM_033380.3(COL4A5):c.874G>A (p.Gly292Arg)	rs104886073
NM_033380.3(COL4A5):c.884G>A (p.Gly295Asp)	rs104886079
NM_033380.3(COL4A5):c.901G>A (p.Gly301Ser)

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