Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 |
11 | g.94476339T= | CA1992433209 | MRE11 | c.609A= (p.Pro203=) c.618A= (p.Pro206=) c.141A= (p.Pro47=) n.905A= | |
11 | g.94476340G>A | CA382376781 | MRE11 | c.608C>T (p.Pro203Leu) c.617C>T (p.Pro206Leu) c.140C>T (p.Pro47Leu) n.904C>T | |
11 | g.94476340G>C | CA382376783 | MRE11 | c.608C>G (p.Pro203Arg) c.617C>G (p.Pro206Arg) c.140C>G (p.Pro47Arg) n.904C>G | |
11 | g.94476340G>T | CA382376786 | MRE11 | c.608C>A (p.Pro203Gln) c.617C>A (p.Pro206Gln) c.140C>A (p.Pro47Gln) n.904C>A | |
11 | g.94476341G>A | CA6235352 | MRE11 | c.607C>T (p.Pro203Ser) c.616C>T (p.Pro206Ser) c.139C>T (p.Pro47Ser) n.903C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.94476341G>C | CA382376789 | MRE11 | c.607C>G (p.Pro203Ala) c.616C>G (p.Pro206Ala) c.139C>G (p.Pro47Ala) n.903C>G | gnomAD v4 |
11 | g.94476341G= | CA1992433218 | MRE11 | c.607C= (p.Pro203=) c.616C= (p.Pro206=) c.139C= (p.Pro47=) n.903C= | |
11 | g.94476341G>T | CA382376792 | MRE11 | c.607C>A (p.Pro203Thr) c.616C>A (p.Pro206Thr) c.139C>A (p.Pro47Thr) n.903C>A | |
11 | g.94476342T>A | CA382376795 | MRE11 | c.606A>T (p.Arg202Ser) c.615A>T (p.Arg205Ser) c.138A>T (p.Arg46Ser) n.902A>T | gnomAD v4 |
11 | g.94476342T>C | CA476286756 | MRE11 | c.606A>G (p.Arg202=) c.615A>G (p.Arg205=) c.138A>G (p.Arg46=) n.902A>G | |
11 | g.94476342T>G | CA382376798 | MRE11 | c.606A>C (p.Arg202Ser) c.615A>C (p.Arg205Ser) c.138A>C (p.Arg46Ser) n.902A>C | |
11 | g.94476343C>A | CA382376807 | MRE11 | c.605G>T (p.Arg202Ile) c.614G>T (p.Arg205Ile) c.137G>T (p.Arg46Ile) n.901G>T | gnomAD v4 |
11 | g.94476343C= | CA1992433228 | MRE11 | c.605G= (p.Arg202=) c.614G= (p.Arg205=) c.137G= (p.Arg46=) n.901G= | |
11 | g.94476343C>G | CA382376805 | MRE11 | c.605G>C (p.Arg202Thr) c.614G>C (p.Arg205Thr) c.137G>C (p.Arg46Thr) n.901G>C | ClinVar |
11 | g.94476343C>T | CA382376801 | MRE11 | c.605G>A (p.Arg202Lys) c.614G>A (p.Arg205Lys) c.137G>A (p.Arg46Lys) n.901G>A | ClinVar dbSNP |
11 | g.94476344T>A | CA382376809 | MRE11 | c.604A>T (p.Arg202Ter) c.613A>T (p.Arg205Ter) c.136A>T (p.Arg46Ter) n.900A>T | |
11 | g.94476344T>C | CA288181 | MRE11 | c.604A>G (p.Arg202Gly) c.613A>G (p.Arg205Gly) c.136A>G (p.Arg46Gly) n.900A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.94476344T>G | CA476286760 | MRE11 | c.604A>C (p.Arg202=) c.613A>C (p.Arg205=) c.136A>C (p.Arg46=) n.900A>C | |
11 | g.94476344T= | CA1992433230 | MRE11 | c.604A= (p.Arg202=) c.613A= (p.Arg205=) c.136A= (p.Arg46=) n.900A= | |
11 | g.94476345C>A | CA382376814 | MRE11 | c.603G>T (p.Leu201Phe) c.612G>T (p.Leu204Phe) c.135G>T (p.Leu45Phe) n.899G>T |