ClinVar Miner

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

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Gene type:
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Total variants: 17
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HGVS dbSNP
NC_000023.11:g.108687666A>G
NM_000495.5(COL4A5):c.1032+17del rs761615270
NM_000495.5(COL4A5):c.1033-15del rs104886089
NM_000495.5(COL4A5):c.1095G>C (p.Gly365=) rs2272945
NM_000495.5(COL4A5):c.1331T>G (p.Ile444Ser) rs2272946
NM_000495.5(COL4A5):c.1588-13T>G rs201708502
NM_000495.5(COL4A5):c.1992G>T (p.Lys664Asn) rs34077552
NM_000495.5(COL4A5):c.2055T>C (p.Leu685=) rs7884085
NM_000495.5(COL4A5):c.2349G>A (p.Pro783=) rs3747408
NM_000495.5(COL4A5):c.2768-11A>G rs1006269
NM_000495.5(COL4A5):c.2858G>T (p.Gly953Val) rs78972735
NM_000495.5(COL4A5):c.3148C>T (p.Pro1050Ser) rs143945573
NM_000495.5(COL4A5):c.3513A>G (p.Gln1171=) rs2273051
NM_000495.5(COL4A5):c.3519T>G (p.Gly1173=) rs61735627
NM_000495.5(COL4A5):c.4275C>T (p.Asp1425=) rs61746140
NM_000495.5(COL4A5):c.609+21T>C rs6622333
NM_000495.5(COL4A5):c.909T>C (p.Asp303=) rs144586397

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