ClinVar Miner

List of variants in gene XRCC2 reported as likely benign by Invitae

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Gene type:
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Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_005431.2(XRCC2):c.678T>C (p.Tyr226=) rs143357617 0.00010
NM_005431.2(XRCC2):c.477C>T (p.Arg159=) rs202226401 0.00008
NM_005431.2(XRCC2):c.282A>G (p.Thr94=) rs376598559 0.00006
NM_005431.2(XRCC2):c.39+8C>G rs200363289 0.00006
NM_005431.2(XRCC2):c.252T>C (p.Asp84=) rs775563874 0.00004
NM_005431.2(XRCC2):c.462T>C (p.Phe154=) rs139923743 0.00004
NM_005431.2(XRCC2):c.669C>T (p.Tyr223=) rs374213093 0.00004
NM_005431.2(XRCC2):c.750C>T (p.Ser250=) rs1171354343 0.00004
NM_005431.2(XRCC2):c.501C>T (p.Asn167=) rs149929851 0.00003
NM_005431.2(XRCC2):c.147A>G (p.Pro49=) rs770063304 0.00002
NM_005431.2(XRCC2):c.225A>G (p.Glu75=) rs751651780 0.00002
NM_005431.2(XRCC2):c.264T>C (p.Asp88=) rs769940007 0.00002
NM_005431.2(XRCC2):c.582G>A (p.Thr194=) rs769829135 0.00002
NM_005431.2(XRCC2):c.102T>C (p.Asp34=) rs1454417236 0.00001
NM_005431.2(XRCC2):c.261T>C (p.Phe87=) rs112146455 0.00001
NM_005431.2(XRCC2):c.39+12C>T rs1057522924 0.00001
NM_005431.2(XRCC2):c.39+13G>A rs750274146 0.00001
NM_005431.2(XRCC2):c.39+9C>T rs2098040921 0.00001
NM_005431.2(XRCC2):c.390T>G (p.Leu130=) rs752735963 0.00001
NM_005431.2(XRCC2):c.432C>T (p.Cys144=) rs1290130026 0.00001
NM_005431.2(XRCC2):c.451C>T (p.Leu151=) rs1396122824 0.00001
NM_005431.2(XRCC2):c.453G>A (p.Leu151=) rs1057522869 0.00001
NM_005431.2(XRCC2):c.456A>C (p.Ser152=) rs758944840 0.00001
NM_005431.2(XRCC2):c.516T>C (p.Thr172=) rs1249442580 0.00001
NM_005431.2(XRCC2):c.528T>C (p.Cys176=) rs765796648 0.00001
NM_005431.2(XRCC2):c.651T>C (p.Cys217=) rs1380848586 0.00001
NM_005431.2(XRCC2):c.777T>C (p.Cys259=) rs138334932 0.00001
NM_005431.2(XRCC2):c.789C>T (p.Asn263=) rs1395130143 0.00001
NM_005431.2(XRCC2):c.828G>A (p.Gly276=) rs1590129146 0.00001
NM_005431.2(XRCC2):c.117G>C (p.Val39=) rs200974031
NM_005431.2(XRCC2):c.121+12A>C rs2116999483
NM_005431.2(XRCC2):c.121+13A>C
NM_005431.2(XRCC2):c.121+13A>G
NM_005431.2(XRCC2):c.121+8A>G rs1057523790
NM_005431.2(XRCC2):c.122-18T>G
NM_005431.2(XRCC2):c.144C>A (p.Gly48=) rs369819565
NM_005431.2(XRCC2):c.144C>T (p.Gly48=) rs369819565
NM_005431.2(XRCC2):c.21G>A (p.Arg7=) rs531499084
NM_005431.2(XRCC2):c.228A>G (p.Val76=) rs1590129740
NM_005431.2(XRCC2):c.234C>T (p.Val78=)
NM_005431.2(XRCC2):c.246T>C (p.Asp82=) rs1590129720
NM_005431.2(XRCC2):c.258C>T (p.His86=) rs1554410545
NM_005431.2(XRCC2):c.270C>G (p.Leu90=) rs2116988188
NM_005431.2(XRCC2):c.30T>C (p.Ser10=) rs1590140912
NM_005431.2(XRCC2):c.339A>C (p.Gly113=) rs1590129640
NM_005431.2(XRCC2):c.360C>T (p.Cys120=) rs1590129609
NM_005431.2(XRCC2):c.39+10G>A
NM_005431.2(XRCC2):c.39+10G>T rs745657340
NM_005431.2(XRCC2):c.39+13G>C rs750274146
NM_005431.2(XRCC2):c.39+20G>A rs2117014350
NM_005431.2(XRCC2):c.40-10_40-8del rs1339890191
NM_005431.2(XRCC2):c.40-17CT[2]
NM_005431.2(XRCC2):c.40-5A>G
NM_005431.2(XRCC2):c.40-5del
NM_005431.2(XRCC2):c.40-6del rs1563030243
NM_005431.2(XRCC2):c.40-8_40-4del rs1590134355
NM_005431.2(XRCC2):c.435T>C (p.Leu145=) rs1454715985
NM_005431.2(XRCC2):c.498G>C (p.Val166=) rs1057521124
NM_005431.2(XRCC2):c.504A>G (p.Leu168=) rs1590129471
NM_005431.2(XRCC2):c.534G>A (p.Gln178=) rs1425124615
NM_005431.2(XRCC2):c.609G>A (p.Ser203=) rs542411586
NM_005431.2(XRCC2):c.612C>T (p.Ser204=)
NM_005431.2(XRCC2):c.636C>G (p.Ala212=)
NM_005431.2(XRCC2):c.654T>C (p.Asp218=) rs2116987268
NM_005431.2(XRCC2):c.675T>G (p.Pro225=)
NM_005431.2(XRCC2):c.690A>G (p.Ala230=)
NM_005431.2(XRCC2):c.699A>G (p.Gln233=) rs3218538
NM_005431.2(XRCC2):c.702G>A (p.Leu234=) rs2116987163
NM_005431.2(XRCC2):c.702G>C (p.Leu234=) rs2116987163
NM_005431.2(XRCC2):c.723C>T (p.Phe241=) rs768994784
NM_005431.2(XRCC2):c.726C>T (p.Ser242=) rs2116987114
NM_005431.2(XRCC2):c.72G>A (p.Leu24=) rs1590134314
NM_005431.2(XRCC2):c.793T>C (p.Leu265=)
NM_005431.2(XRCC2):c.801A>G (p.Lys267=) rs1433853429

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