Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.94476325T>A | CA382376681 | MRE11 | c.623A>T (p.Asn208Ile) c.632A>T (p.Asn211Ile) c.155A>T (p.Asn52Ile) n.919A>T | |
11 | g.94476325T>C | CA382376682 | MRE11 | c.623A>G (p.Asn208Ser) c.632A>G (p.Asn211Ser) c.155A>G (p.Asn52Ser) n.919A>G | |
11 | g.94476325T>G | CA382376683 | MRE11 | c.623A>C (p.Asn208Thr) c.632A>C (p.Asn211Thr) c.155A>C (p.Asn52Thr) n.919A>C | |
11 | g.94476326T>A | CA382376685 | MRE11 | c.622A>T (p.Asn208Tyr) c.631A>T (p.Asn211Tyr) c.154A>T (p.Asn52Tyr) n.918A>T | |
11 | g.94476326T>C | CA382376688 | MRE11 | c.622A>G (p.Asn208Asp) c.631A>G (p.Asn211Asp) c.154A>G (p.Asn52Asp) n.918A>G | |
11 | g.94476326T>G | CA382376689 | MRE11 | c.622A>C (p.Asn208His) c.631A>C (p.Asn211His) c.154A>C (p.Asn52His) n.918A>C | ClinVar |
11 | g.94476327C>A | CA382376690 | MRE11 | c.621G>T (p.Glu207Asp) c.630G>T (p.Glu210Asp) c.153G>T (p.Glu51Asp) n.917G>T | |
11 | g.94476327C>G | CA382376693 | MRE11 | c.621G>C (p.Glu207Asp) c.630G>C (p.Glu210Asp) c.153G>C (p.Glu51Asp) n.917G>C | ClinVar |
11 | g.94476327C>T | CA476286749 | MRE11 | c.621G>A (p.Glu207=) c.630G>A (p.Glu210=) c.153G>A (p.Glu51=) n.917G>A | ClinVar |
11 | g.94476328T>A | CA382376697 | MRE11 | c.620A>T (p.Glu207Val) c.629A>T (p.Glu210Val) c.152A>T (p.Glu51Val) n.916A>T | |
11 | g.94476328T>C | CA382376699 | MRE11 | c.620A>G (p.Glu207Gly) c.629A>G (p.Glu210Gly) c.152A>G (p.Glu51Gly) n.916A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.94476328T>G | CA382376702 | MRE11 | c.620A>C (p.Glu207Ala) c.629A>C (p.Glu210Ala) c.152A>C (p.Glu51Ala) n.916A>C | |
11 | g.94476328T= | CA1992433175 | MRE11 | c.620A= (p.Glu207=) c.629A= (p.Glu210=) c.152A= (p.Glu51=) n.916A= | |
11 | g.94476329C>A | CA382376704 | MRE11 | c.619G>T (p.Glu207Ter) c.628G>T (p.Glu210Ter) c.151G>T (p.Glu51Ter) n.915G>T | |
11 | g.94476329C>G | CA382376706 | MRE11 | c.619G>C (p.Glu207Gln) c.628G>C (p.Glu210Gln) c.151G>C (p.Glu51Gln) n.915G>C | |
11 | g.94476329C>T | CA382376708 | MRE11 | c.619G>A (p.Glu207Lys) c.628G>A (p.Glu210Lys) c.151G>A (p.Glu51Lys) n.915G>A | |
11 | g.94476330A= | CA1992433194 | MRE11 | c.618T= (p.Asp206=) c.627T= (p.Asp209=) c.150T= (p.Asp50=) n.914T= | |
11 | g.94476330A>C | CA382376710 | MRE11 | c.618T>G (p.Asp206Glu) c.627T>G (p.Asp209Glu) c.150T>G (p.Asp50Glu) n.914T>G | |
11 | g.94476330A>G | CA188823 | MRE11 | c.618T>C (p.Asp206=) c.627T>C (p.Asp209=) c.150T>C (p.Asp50=) n.914T>C | ClinVar dbSNP gnomAD v4 |
11 | g.94476330A>T | CA382376715 | MRE11 | c.618T>A (p.Asp206Glu) c.627T>A (p.Asp209Glu) c.150T>A (p.Asp50Glu) n.914T>A | |
11 | g.94476331T>A | CA382376718 | MRE11 | c.617A>T (p.Asp206Val) c.626A>T (p.Asp209Val) c.149A>T (p.Asp50Val) n.913A>T | |
11 | g.94476331T>C | CA382376720 | MRE11 | c.617A>G (p.Asp206Gly) c.626A>G (p.Asp209Gly) c.149A>G (p.Asp50Gly) n.913A>G | ClinVar |
11 | g.94476331T>G | CA382376723 | MRE11 | c.617A>C (p.Asp206Ala) c.626A>C (p.Asp209Ala) c.149A>C (p.Asp50Ala) n.913A>C | dbSNP |
11 | g.94476331T= | CA1992433196 | MRE11 | c.617A= (p.Asp206=) c.626A= (p.Asp209=) c.149A= (p.Asp50=) n.913A= | |
11 | g.94476332C>A | CA382376726 | MRE11 | c.616G>T (p.Asp206Tyr) c.625G>T (p.Asp209Tyr) c.148G>T (p.Asp50Tyr) n.912G>T | COSMIC COSMIC |
11 | g.94476332C>G | CA382376732 | MRE11 | c.616G>C (p.Asp206His) c.625G>C (p.Asp209His) c.148G>C (p.Asp50His) n.912G>C | |
11 | g.94476332C>T | CA382376728 | MRE11 | c.616G>A (p.Asp206Asn) c.625G>A (p.Asp209Asn) c.148G>A (p.Asp50Asn) n.912G>A | dbSNP |
11 | g.94476333T>A | CA382376734 | MRE11 | c.615A>T (p.Glu205Asp) c.624A>T (p.Glu208Asp) c.147A>T (p.Glu49Asp) n.911A>T | dbSNP |
11 | g.94476333T>C | CA476286751 | MRE11 | c.615A>G (p.Glu205=) c.624A>G (p.Glu208=) c.147A>G (p.Glu49=) n.911A>G | gnomAD v4 |
11 | g.94476333T>G | CA382376737 | MRE11 | c.615A>C (p.Glu205Asp) c.624A>C (p.Glu208Asp) c.147A>C (p.Glu49Asp) n.911A>C | |
11 | g.94476334T>A | CA382376741 | MRE11 | c.614A>T (p.Glu205Val) c.623A>T (p.Glu208Val) c.146A>T (p.Glu49Val) n.910A>T | |
11 | g.94476334T>C | CA382376743 | MRE11 | c.614A>G (p.Glu205Gly) c.623A>G (p.Glu208Gly) c.146A>G (p.Glu49Gly) n.910A>G | |
11 | g.94476334T>G | CA382376746 | MRE11 | c.614A>C (p.Glu205Ala) c.623A>C (p.Glu208Ala) c.146A>C (p.Glu49Ala) n.910A>C | |
11 | g.94476335C>A | CA382376749 | MRE11 | c.613G>T (p.Glu205Ter) c.622G>T (p.Glu208Ter) c.145G>T (p.Glu49Ter) n.909G>T | |
11 | g.94476335C>G | CA382376751 | MRE11 | c.613G>C (p.Glu205Gln) c.622G>C (p.Glu208Gln) c.145G>C (p.Glu49Gln) n.909G>C | |
11 | g.94476335C>T | CA382376752 | MRE11 | c.613G>A (p.Glu205Lys) c.622G>A (p.Glu208Lys) c.145G>A (p.Glu49Lys) n.909G>A | |
11 | g.94476336C>A | CA382376754 | MRE11 | c.612G>T (p.Lys204Asn) c.621G>T (p.Lys207Asn) c.144G>T (p.Lys48Asn) n.908G>T | |
11 | g.94476336C>G | CA382376757 | MRE11 | c.612G>C (p.Lys204Asn) c.621G>C (p.Lys207Asn) c.144G>C (p.Lys48Asn) n.908G>C | |
11 | g.94476336C>T | CA476286752 | MRE11 | c.612G>A (p.Lys204=) c.621G>A (p.Lys207=) c.144G>A (p.Lys48=) n.908G>A | gnomAD v4 |
11 | g.94476337T>A | CA382376764 | MRE11 | c.611A>T (p.Lys204Met) c.620A>T (p.Lys207Met) c.143A>T (p.Lys48Met) n.907A>T | |
11 | g.94476337T>C | CA10579404 | MRE11 | c.611A>G (p.Lys204Arg) c.620A>G (p.Lys207Arg) c.143A>G (p.Lys48Arg) n.907A>G | ClinVar dbSNP |
11 | g.94476337T>G | CA382376769 | MRE11 | c.611A>C (p.Lys204Thr) c.620A>C (p.Lys207Thr) c.143A>C (p.Lys48Thr) n.907A>C | |
11 | g.94476337T= | CA1992433198 | MRE11 | c.611A= (p.Lys204=) c.620A= (p.Lys207=) c.143A= (p.Lys48=) n.907A= | |
11 | g.94476338T>A | CA382376772 | MRE11 | c.610A>T (p.Lys204Ter) c.619A>T (p.Lys207Ter) c.142A>T (p.Lys48Ter) n.906A>T | |
11 | g.94476338T>C | CA382376776 | MRE11 | c.610A>G (p.Lys204Glu) c.619A>G (p.Lys207Glu) c.142A>G (p.Lys48Glu) n.906A>G | dbSNP |
11 | g.94476338T>G | CA382376773 | MRE11 | c.610A>C (p.Lys204Gln) c.619A>C (p.Lys207Gln) c.142A>C (p.Lys48Gln) n.906A>C | |
11 | g.94476338T= | CA1992433205 | MRE11 | c.610A= (p.Lys204=) c.619A= (p.Lys207=) c.142A= (p.Lys48=) n.906A= | |
11 | g.94476339T>A | CA476286754 | MRE11 | c.609A>T (p.Pro203=) c.618A>T (p.Pro206=) c.141A>T (p.Pro47=) n.905A>T | |
11 | g.94476339T>C | CA476286755 | MRE11 | c.609A>G (p.Pro203=) c.618A>G (p.Pro206=) c.141A>G (p.Pro47=) n.905A>G | gnomAD v4 |
11 | g.94476339T>G | CA6235351 | MRE11 | c.609A>C (p.Pro203=) c.618A>C (p.Pro206=) c.141A>C (p.Pro47=) n.905A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |