List of variants in gene combination ERCC4, LOC130058543 reported as likely benign for Xeroderma pigmentosum, group F; Cockayne syndrome; Fanconi anemia complementation group Q

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_005236.3(ERCC4):c.69G>A (p.Val23=)	rs201606798	0.00003
NM_005236.3(ERCC4):c.105C>T (p.Cys35=)	rs762885804	0.00002
NM_005236.3(ERCC4):c.15G>A (p.Gln5=)	rs748509102	0.00001
NM_005236.3(ERCC4):c.114G>A (p.Gly38=)
NM_005236.3(ERCC4):c.129G>A (p.Arg43=)
NM_005236.3(ERCC4):c.132C>T (p.Leu44=)	rs1482378244
NM_005236.3(ERCC4):c.147C>T (p.Leu49=)
NM_005236.3(ERCC4):c.165A>G (p.Pro55=)
NM_005236.3(ERCC4):c.178C>T (p.Leu60=)	rs2141937412
NM_005236.3(ERCC4):c.183G>A (p.Val61=)	rs1215558892
NM_005236.3(ERCC4):c.22C>A (p.Arg8=)	rs774510191
NM_005236.3(ERCC4):c.42G>A (p.Pro14=)	rs2141936987
NM_005236.3(ERCC4):c.43C>T (p.Leu15=)
NM_005236.3(ERCC4):c.81C>T (p.Leu27=)
NM_005236.3(ERCC4):c.96A>G (p.Leu32=)
NM_005236.3(ERCC4):c.9A>C (p.Ser3=)

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