List of variants in gene combination BIVM-ERCC5, ERCC5 reported as likely pathogenic for female reproductive organ cancer

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000123.4(ERCC5):c.1156C>T (p.Arg386Trp)	rs758046666	0.00004
NM_000123.4(ERCC5):c.11A>C (p.Gln4Pro)
NM_000123.4(ERCC5):c.3256G>C (p.Gly1086Arg)
NM_000123.4(ERCC5):c.878A>T (p.Lys293Ile)
NM_000123.4(ERCC5):c.92T>C (p.Ile31Thr)

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