ClinVar Miner

List of variants in gene COL4A4 reported as likely benign for not specified

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_000092.5(COL4A4):c.1781A>G (p.Glu594Gly) rs35998949 0.02275
NM_000092.5(COL4A4):c.-15T>C rs17353916 0.00433
NM_000092.5(COL4A4):c.50A>G (p.Lys17Arg) rs114969026 0.00341
NM_000092.5(COL4A4):c.5016A>G (p.Glu1672=) rs34761049 0.00264
NM_000092.5(COL4A4):c.4217-15T>C rs200926310 0.00228
NM_000092.5(COL4A4):c.4090+14T>C rs147376687 0.00207
NM_000092.5(COL4A4):c.2056+10A>G rs138869451 0.00161
NM_000092.5(COL4A4):c.195T>C (p.Gly65=) rs201278620 0.00082
NM_000092.5(COL4A4):c.2241C>T (p.Pro747=) rs374510402 0.00048
NM_000092.5(COL4A4):c.4349T>C (p.Ile1450Thr) rs72969704 0.00038
NM_000092.5(COL4A4):c.3666T>C (p.Pro1222=) rs372838090 0.00029
NM_000092.5(COL4A4):c.1435G>C (p.Gly479Arg) rs202210475 0.00026
NM_000092.5(COL4A4):c.4674G>A (p.Ala1558=) rs373933029 0.00021
NM_000092.5(COL4A4):c.2430C>G (p.Gly810=) rs769363556 0.00015
NM_000092.5(COL4A4):c.3995C>T (p.Pro1332Leu) rs200860702 0.00009
NM_000092.5(COL4A4):c.928C>T (p.Arg310Trp) rs200817090 0.00005
NM_000092.5(COL4A4):c.291C>T (p.Arg97=) rs749441530 0.00003
NM_000092.5(COL4A4):c.888G>A (p.Gly296=) rs746239973 0.00003
NM_000092.5(COL4A4):c.1308G>C (p.Gly436=)
NM_000092.5(COL4A4):c.2319G>A (p.Arg773=) rs200920187
NM_000092.5(COL4A4):c.2529G>A (p.Gly843=) rs886038229
NM_000092.5(COL4A4):c.2647C>A (p.Pro883Thr) rs200761108
NM_000092.5(COL4A4):c.297T>A (p.Pro99=) rs1576662029
NM_000092.5(COL4A4):c.3215-18G>T rs886038230
NM_000092.5(COL4A4):c.372+13A>T
NM_000092.5(COL4A4):c.4081+18A>G
NM_000092.5(COL4A4):c.4334-3del rs780415519
NM_000092.5(COL4A4):c.4485C>T (p.Tyr1495=) rs1553613757
NM_000092.5(COL4A4):c.4760C>G (p.Pro1587Arg) rs190148408
NM_000092.5(COL4A4):c.4809+14C>T
NM_000092.5(COL4A4):c.870+19T>C
NM_000092.5(COL4A4):c.99A>T (p.Val33=) rs886038231

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