Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.230710725G>A | CA1448382 | AGT | c.99C>T (p.His33=) n.610C>T c.126C>T (p.His42=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.230710725G>C | CA1448383 | AGT | c.99C>G (p.His33Gln) n.610C>G c.126C>G (p.His42Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.230710725G= | CA1226658824 | AGT | c.99C= (p.His33=) n.610C= c.126C= (p.His42=) | |
1 | g.230710725G>T | CA345207668 | AGT | c.99C>A (p.His33Gln) n.610C>A c.126C>A (p.His42Gln) | |
1 | g.230710726T>A | CA345207671 | AGT | c.98A>T (p.His33Leu) n.609A>T c.125A>T (p.His42Leu) | |
1 | g.230710726T>C | CA345207672 | AGT | c.98A>G (p.His33Arg) n.609A>G c.125A>G (p.His42Arg) | |
1 | g.230710726T>G | CA345207673 | AGT | c.98A>C (p.His33Pro) n.609A>C c.125A>C (p.His42Pro) | |
1 | g.230710727G>A | CA345207674 | AGT | c.97C>T (p.His33Tyr) n.608C>T c.124C>T (p.His42Tyr) | |
1 | g.230710727G>C | CA345207676 | AGT | c.97C>G (p.His33Asp) n.608C>G c.124C>G (p.His42Asp) | |
1 | g.230710727G>T | CA345207678 | AGT | c.97C>A (p.His33Asn) n.608C>A c.124C>A (p.His42Asn) | |
1 | g.230710728G>A | CA424036990 | AGT | c.96C>T (p.Phe32=) n.607C>T c.123C>T (p.Phe41=) | |
1 | g.230710728G>C | CA345207679 | AGT | c.96C>G (p.Phe32Leu) n.607C>G c.123C>G (p.Phe41Leu) | |
1 | g.230710728G>T | CA345207681 | AGT | c.96C>A (p.Phe32Leu) n.607C>A c.123C>A (p.Phe41Leu) | |
1 | g.230710729A>C | CA345207686 | AGT | c.95T>G (p.Phe32Cys) n.606T>G c.122T>G (p.Phe41Cys) | |
1 | g.230710729A>G | CA345207685 | AGT | c.95T>C (p.Phe32Ser) n.606T>C c.122T>C (p.Phe41Ser) | gnomAD v4 |
1 | g.230710729A>T | CA345207683 | AGT | c.95T>A (p.Phe32Tyr) n.606T>A c.122T>A (p.Phe41Tyr) | |
1 | g.230710730A>C | CA345207688 | AGT | c.94T>G (p.Phe32Val) n.605T>G c.121T>G (p.Phe41Val) | |
1 | g.230710730A>G | CA345207690 | AGT | c.94T>C (p.Phe32Leu) n.605T>C c.121T>C (p.Phe41Leu) | gnomAD v4 |
1 | g.230710730A>T | CA345207692 | AGT | c.94T>A (p.Phe32Ile) n.605T>A c.121T>A (p.Phe41Ile) | |
1 | g.230710731G>A | CA424036993 | AGT | c.93C>T (p.Pro31=) n.604C>T c.120C>T (p.Pro40=) | gnomAD v4 |
1 | g.230710731G>C | CA424036994 | AGT | c.93C>G (p.Pro31=) n.604C>G c.120C>G (p.Pro40=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.230710731G= | CA1226658828 | AGT | c.93C= (p.Pro31=) n.604C= c.120C= (p.Pro40=) | |
1 | g.230710731G>T | CA424036995 | AGT | c.93C>A (p.Pro31=) n.604C>A c.120C>A (p.Pro40=) | |
1 | g.230710732G>A | CA1448384 | AGT | c.92C>T (p.Pro31Leu) n.603C>T c.119C>T (p.Pro40Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.230710732G>C | CA345207694 | AGT | c.92C>G (p.Pro31Arg) n.603C>G c.119C>G (p.Pro40Arg) | |
1 | g.230710732G= | CA1148399829 | AGT | c.92C= (p.Pro31=) n.603C= c.119C= (p.Pro40=) | |
1 | g.230710732G>T | CA345207696 | AGT | c.92C>A (p.Pro31His) n.603C>A c.119C>A (p.Pro40His) | gnomAD v4 |
1 | g.230710733G>A | CA345207698 | AGT | c.91C>T (p.Pro31Ser) n.602C>T c.118C>T (p.Pro40Ser) | |
1 | g.230710733G>C | CA345207700 | AGT | c.91C>G (p.Pro31Ala) n.602C>G c.118C>G (p.Pro40Ala) | |
1 | g.230710733G= | CA1226658839 | AGT | c.91C= (p.Pro31=) n.602C= c.118C= (p.Pro40=) | |
1 | g.230710733G>T | CA38872442 | AGT | c.91C>A (p.Pro31Thr) n.602C>A c.118C>A (p.Pro40Thr) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.230710734G>A | CA1448385 | AGT | c.90C>T (p.His30=) n.601C>T c.117C>T (p.His39=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.230710734G>C | CA345207703 | AGT | c.90C>G (p.His30Gln) n.601C>G c.117C>G (p.His39Gln) | |
1 | g.230710734G= | CA1144110391 | AGT | c.90C= (p.His30=) n.601C= c.117C= (p.His39=) | |
1 | g.230710734G>T | CA345207704 | AGT | c.90C>A (p.His30Gln) n.601C>A c.117C>A (p.His39Gln) | |
1 | g.230710735T>A | CA345207708 | AGT | c.89A>T (p.His30Leu) n.600A>T c.116A>T (p.His39Leu) | |
1 | g.230710735T>C | CA38872445 | AGT | c.89A>G (p.His30Arg) n.600A>G c.116A>G (p.His39Arg) | dbSNP gnomAD v4 |
1 | g.230710735T>G | CA345207706 | AGT | c.89A>C (p.His30Pro) n.600A>C c.116A>C (p.His39Pro) | dbSNP |
1 | g.230710735T= | CA1145147796 | AGT | c.89A= (p.His30=) n.600A= c.116A= (p.His39=) | |
1 | g.230710736G>A | CA345207711 | AGT | c.88C>T (p.His30Tyr) n.599C>T c.115C>T (p.His39Tyr) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.230710736G>C | CA345207712 | AGT | c.88C>G (p.His30Asp) n.599C>G c.115C>G (p.His39Asp) | |
1 | g.230710736G= | CA1226658845 | AGT | c.88C= (p.His30=) n.599C= c.115C= (p.His39=) | |
1 | g.230710736G>T | CA345207714 | AGT | c.88C>A (p.His30Asn) n.599C>A c.115C>A (p.His39Asn) | |
1 | g.230710737T>A | CA424037003 | AGT | c.87A>T (p.Ile29=) n.598A>T c.114A>T (p.Ile38=) | |
1 | g.230710737T>C | CA345207716 | AGT | c.87A>G (p.Ile29Met) n.598A>G c.114A>G (p.Ile38Met) | |
1 | g.230710737T>G | CA424037004 | AGT | c.87A>C (p.Ile29=) n.598A>C c.114A>C (p.Ile38=) | gnomAD v4 |
1 | g.230710738A>C | CA345207718 | AGT | c.86T>G (p.Ile29Arg) n.597T>G c.113T>G (p.Ile38Arg) | |
1 | g.230710738A>G | CA345207720 | AGT | c.86T>C (p.Ile29Thr) n.597T>C c.113T>C (p.Ile38Thr) | |
1 | g.230710738A>T | CA345207722 | AGT | c.86T>A (p.Ile29Lys) n.597T>A c.113T>A (p.Ile38Lys) | COSMIC |
1 | g.230710739T>A | CA345207723 | AGT | c.85A>T (p.Ile29Leu) n.596A>T c.112A>T (p.Ile38Leu) |