List of variants in gene COL4A5 reported as likely benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_033380.3(COL4A5):c.1331T>G (p.Ile444Ser)	rs2272946	0.11020
NM_033380.3(COL4A5):c.1289C>A (p.Ala430Asp)	rs142883891	0.00418
NM_033380.3(COL4A5):c.2215C>G (p.Pro739Ala)	rs104886164	0.00034
NM_033380.3(COL4A5):c.4353A>T (p.Gly1451=)	rs146884759	0.00028
NM_033380.3(COL4A5):c.2979T>G (p.Pro993=)	rs41306255	0.00024
NM_033380.3(COL4A5):c.3426C>T (p.Pro1142=)	rs780896516	0.00019
NM_033380.3(COL4A5):c.3107-11A>T	rs190579028	0.00015
NM_033380.3(COL4A5):c.488T>C (p.Met163Thr)	rs142503631	0.00012
NM_033380.3(COL4A5):c.2286A>G (p.Pro762=)	rs369726425	0.00008
NM_033380.3(COL4A5):c.2604C>T (p.Pro868=)	rs781337825	0.00003
NM_033380.3(COL4A5):c.2395+4T>C	rs774352105	0.00002
NM_033380.3(COL4A5):c.2865G>A (p.Met955Ile)	rs1350078739	0.00001
NM_033380.3(COL4A5):c.1608T>A (p.Gly536=)
NM_033380.3(COL4A5):c.2109C>T (p.Ile703=)	rs369092053
NM_033380.3(COL4A5):c.2917+17A>G
NM_033380.3(COL4A5):c.3554-5G>C	rs1057522041
NM_033380.3(COL4A5):c.3604+19T>A
NM_033380.3(COL4A5):c.406A>G (p.Ser136Gly)	rs768580195
NM_033380.3(COL4A5):c.4092T>C (p.Pro1364=)
NM_033380.3(COL4A5):c.465+12A>T

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