ClinVar Miner

List of variants in gene combination FANCA, ZNF276 studied for not specified

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_001113525.2(ZNF276):c.*1693A>T rs7195906 0.53795
NM_001113525.2(ZNF276):c.*1323G>A rs1061646 0.40513
NM_001113525.2(ZNF276):c.*1689C>A rs11647746 0.11315
NM_000135.4(FANCA):c.3807G>C (p.Leu1269=) rs11649210 0.11105
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_001113525.2(ZNF276):c.*1316C>T rs9282680 0.01028
NM_000135.4(FANCA):c.4249C>G (p.His1417Asp) rs17227403 0.00362
NM_000135.4(FANCA):c.3891G>A (p.Lys1297=) rs17227361 0.00286
NM_001113525.2(ZNF276):c.*841G>A rs191404781 0.00092
NM_000135.4(FANCA):c.4332T>G (p.Pro1444=) rs149531696 0.00072
NM_000135.4(FANCA):c.4036G>A (p.Ala1346Thr) rs17227396 0.00056
NM_001113525.2(ZNF276):c.*470A>C rs372268907 0.00049
NM_000135.4(FANCA):c.3981C>T (p.His1327=) rs141278771 0.00036
NM_000135.4(FANCA):c.3912A>G (p.Ala1304=) rs545021222 0.00019
NM_001113525.2(ZNF276):c.*1674G>C rs56216970 0.00016
NM_000135.4(FANCA):c.4015C>T (p.Leu1339Phe) rs149775657 0.00015
NM_001113525.2(ZNF276):c.*1313A>G rs368376237 0.00012
NM_000135.4(FANCA):c.3810G>A (p.Ser1270=) rs138144828 0.00009
NM_000135.4(FANCA):c.3950G>A (p.Arg1317Gln) rs376523966 0.00006
NM_000135.4(FANCA):c.4226G>A (p.Arg1409Gln) rs370507983 0.00006
NM_000135.4(FANCA):c.4232C>T (p.Pro1411Leu) rs201494304 0.00006
NM_000135.4(FANCA):c.4273C>T (p.Arg1425Cys) rs587778321 0.00006
NM_000135.4(FANCA):c.3997T>C (p.Phe1333Leu) rs576079738 0.00004
NM_000135.4(FANCA):c.4241G>A (p.Ser1414Asn) rs772122405 0.00002
NM_000135.4(FANCA):c.3857A>C (p.His1286Pro) rs138620653 0.00001
NM_000135.4(FANCA):c.3972G>C (p.Pro1324=) rs1446370085 0.00001
NM_000135.4(FANCA):c.4274G>A (p.Arg1425His) rs147406377 0.00001
NM_001113525.2(ZNF276):c.*348G>A rs1458061374 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.3877G>A (p.Glu1293Lys) rs1015729981
NM_000135.4(FANCA):c.3901T>A (p.Ser1301Thr) rs765162125
NM_000135.4(FANCA):c.3953TCC[2] (p.Leu1320del) rs927201841
NM_000135.4(FANCA):c.3983C>T (p.Thr1328Ile) rs587778320
NM_000135.4(FANCA):c.4309C>T (p.Gln1437Ter)
NM_000135.4(FANCA):c.4316G>C (p.Arg1439Thr) rs587778322
NM_001113525.2(ZNF276):c.*607A>G rs1800359
NM_001113525.2(ZNF276):c.*631G>A

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