List of variants in gene combination FANCA, ZNF276 reported by ITMI

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001113525.2(ZNF276):c.*1693A>T	rs7195906	0.53795
NM_001113525.2(ZNF276):c.*1689C>A	rs11647746	0.11315
NM_000135.4(FANCA):c.3982A>G (p.Thr1328Ala)	rs9282681	0.05868
NM_000135.4(FANCA):c.3859G>A (p.Val1287Ile)	rs17227354	0.02526
NM_000135.4(FANCA):c.4249C>G (p.His1417Asp)	rs17227403	0.00362
NM_000135.4(FANCA):c.4036G>A (p.Ala1346Thr)	rs17227396	0.00056
NM_001113525.2(ZNF276):c.*1674G>C	rs56216970	0.00016
NM_000135.4(FANCA):c.4015C>T (p.Leu1339Phe)	rs149775657	0.00015
NM_000135.4(FANCA):c.4226G>A (p.Arg1409Gln)	rs370507983	0.00006
NM_000135.4(FANCA):c.4273C>T (p.Arg1425Cys)	rs587778321	0.00006
NM_000135.4(FANCA):c.3857A>C (p.His1286Pro)	rs138620653	0.00001
NM_000135.4(FANCA):c.3782TCT[2] (p.Phe1263del)	rs397507553
NM_000135.4(FANCA):c.3792del (p.Ser1264_Leu1265insTer)	rs587778319
NM_000135.4(FANCA):c.3983C>T (p.Thr1328Ile)	rs587778320
NM_000135.4(FANCA):c.4316G>C (p.Arg1439Thr)	rs587778322

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