ClinVar Miner

List of variants reported as uncertain significance for Xeroderma pigmentosum group B by Illumina Laboratory Services, Illumina

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_000122.2(ERCC3):c.847C>T (p.Arg283Cys) rs145201970 0.00142
NM_000122.2(ERCC3):c.822+14C>T rs200833462 0.00092
NM_000122.2(ERCC3):c.2080G>A (p.Ala694Thr) rs151216904 0.00082
NM_000122.2(ERCC3):c.618C>T (p.Ala206=) rs145830873 0.00077
NM_000122.2(ERCC3):c.144G>C (p.Glu48Asp) rs149309991 0.00048
NM_000122.2(ERCC3):c.1411G>A (p.Val471Ile) rs371627165 0.00029
NM_000122.2(ERCC3):c.314A>G (p.Glu105Gly) rs116713511 0.00025
NM_000122.2(ERCC3):c.2226G>A (p.Arg742=) rs376593226 0.00022
NM_000122.2(ERCC3):c.1155C>T (p.Asp385=) rs371396764 0.00017
NM_000122.2(ERCC3):c.2218-5G>A rs201054106 0.00016
NM_000122.2(ERCC3):c.2087T>G (p.Met696Arg) rs201806429 0.00011
NM_000122.2(ERCC3):c.2106G>A (p.Ala702=) rs114508982 0.00011
NM_000122.2(ERCC3):c.1078C>T (p.Arg360Cys) rs754010782 0.00009
NM_000122.2(ERCC3):c.2224C>T (p.Arg742Trp) rs368664230 0.00009
NM_000122.2(ERCC3):c.1076A>G (p.Lys359Arg) rs370519739 0.00007
NM_000122.2(ERCC3):c.254T>G (p.Phe85Cys) rs767507847 0.00007
NM_000122.2(ERCC3):c.529G>A (p.Val177Ile) rs139690693 0.00007
NM_000122.2(ERCC3):c.1182C>T (p.Ser394=) rs377391723 0.00006
NM_000122.2(ERCC3):c.385G>A (p.Val129Ile) rs145762413 0.00005
NM_000122.2(ERCC3):c.*138G>C rs545297258 0.00004
NM_000122.2(ERCC3):c.1026C>T (p.Cys342=) rs752026166 0.00003
NM_000122.2(ERCC3):c.1731-11T>C rs746754189 0.00003
NM_000122.2(ERCC3):c.2218-6C>T rs200733704 0.00003
NM_000122.2(ERCC3):c.359C>T (p.Ala120Val) rs370115857 0.00003
NM_000122.2(ERCC3):c.1110T>C (p.Ser370=) rs774063464 0.00002
NM_000122.2(ERCC3):c.1929G>T (p.Val643=) rs375556869 0.00002
NM_000122.2(ERCC3):c.28+8G>A rs886054844 0.00002
NM_000122.2(ERCC3):c.-31G>A rs766435259 0.00001
NM_000122.2(ERCC3):c.1156G>A (p.Asp386Asn) rs374264195 0.00001
NM_000122.2(ERCC3):c.131A>G (p.Lys44Arg) rs771345526 0.00001
NM_000122.2(ERCC3):c.1371C>T (p.Ile457=) rs769083884 0.00001
NM_000122.2(ERCC3):c.1911C>G (p.Ala637=) rs1258857605 0.00001
NM_000122.2(ERCC3):c.1986G>A (p.Leu662=) rs1419254389 0.00001
NM_000122.2(ERCC3):c.657+15G>A rs781533251 0.00001
NM_000122.2(ERCC3):c.*220G>C rs1684042791
NM_000122.2(ERCC3):c.*83C>T rs1684047924
NM_000122.2(ERCC3):c.1152T>C (p.Ile384=) rs1194673433
NM_000122.2(ERCC3):c.2080G>T (p.Ala694Ser) rs151216904
NM_000122.2(ERCC3):c.2112G>A (p.Ser704=) rs114710997

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