List of variants in gene COL4A5 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 38

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HGVS	dbSNP	gnomAD frequency
NM_033380.3(COL4A5):c.1289C>A (p.Ala430Asp)	rs142883891	0.00418
NM_033380.3(COL4A5):c.3148C>T (p.Pro1050Ser)	rs143945573	0.00155
NM_033380.3(COL4A5):c.2147-12A>G	rs749368555	0.00061
NM_033380.3(COL4A5):c.1187C>T (p.Pro396Leu)	rs113013606	0.00047
NM_033380.3(COL4A5):c.1588-13T>G	rs201708502	0.00047
NM_033380.3(COL4A5):c.3312T>C (p.Gly1104=)	rs140829723	0.00032
NM_033380.3(COL4A5):c.2244+9C>T	rs759349551	0.00027
NM_033380.3(COL4A5):c.2917+18T>C	rs376067886	0.00023
NM_033380.3(COL4A5):c.2400T>C (p.Asp800=)	rs372505008	0.00021
NM_033380.3(COL4A5):c.4015+5T>C	rs190856675	0.00020
NM_033380.3(COL4A5):c.1979C>T (p.Thr660Ile)	rs780612276	0.00019
NM_033380.3(COL4A5):c.4117C>A (p.Gln1373Lys)	rs147447379	0.00014
NM_033380.3(COL4A5):c.2571A>G (p.Gly857=)	rs41311553	0.00012
NM_033380.3(COL4A5):c.4315+9A>T	rs764116323	0.00012
NM_033380.3(COL4A5):c.488T>C (p.Met163Thr)	rs142503631	0.00012
NM_033380.3(COL4A5):c.4075A>G (p.Ile1359Val)	rs748850424	0.00009
NM_033380.3(COL4A5):c.1497A>G (p.Pro499=)	rs772348542	0.00007
NM_033380.3(COL4A5):c.3247-10G>A	rs369817184	0.00007
NM_033380.3(COL4A5):c.646-6C>T	rs200151467	0.00007
NM_033380.3(COL4A5):c.528A>G (p.Pro176=)	rs780845413	0.00006
NM_033380.3(COL4A5):c.2348C>T (p.Pro783Leu)	rs747288279	0.00005
NM_033380.3(COL4A5):c.4309C>G (p.Gln1437Glu)	rs143778018	0.00005
NM_033380.3(COL4A5):c.3993C>T (p.Leu1331=)	rs751858178	0.00004
NM_033380.3(COL4A5):c.1469C>T (p.Ser490Leu)	rs764543034	0.00003
NM_033380.3(COL4A5):c.1909C>A (p.Gln637Lys)	rs368347660	0.00003
NM_033380.3(COL4A5):c.2797C>T (p.Leu933Phe)	rs191497639	0.00003
NM_033380.3(COL4A5):c.892-4A>G	rs777914438	0.00003
NM_033380.3(COL4A5):c.1546G>C (p.Glu516Gln)	rs770915647	0.00002
NM_033380.3(COL4A5):c.4016-16T>G	rs775007873	0.00002
NM_033380.3(COL4A5):c.1423+10C>T	rs1161395968	0.00001
NM_033380.3(COL4A5):c.2466A>G (p.Gly822=)	rs375746429	0.00001
NM_033380.3(COL4A5):c.2667T>C (p.Ser889=)	rs1258505968	0.00001
NM_033380.3(COL4A5):c.1032+17del	rs761615270
NM_033380.3(COL4A5):c.1530C>T (p.Phe510=)	rs2147809019
NM_033380.3(COL4A5):c.3357C>A (p.Gly1119=)	rs773019423
NM_033380.3(COL4A5):c.4247G>A (p.Arg1416His)	rs753765957
NM_033380.3(COL4A5):c.4282C>T (p.Arg1428Cys)	rs144282156
NM_033380.3(COL4A5):c.892-16del	rs775131776

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