Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.8059732C>A | CA383798903 | C3AR1 | c.454G>T (p.Val152Leu) | |
12 | g.8059732C>G | CA383798904 | C3AR1 | c.454G>C (p.Val152Leu) | |
12 | g.8059732C>T | CA383798905 | C3AR1 | c.454G>A (p.Val152Met) | |
12 | g.8059732_8059733delinsCA | CA2014849546 | C3AR1 | c.453_454delinsTG (p.Phe151=) | |
12 | g.8059733A>C | CA383798906 | C3AR1 | c.453T>G (p.Phe151Leu) | |
12 | g.8059733A>G | CA478528884 | C3AR1 | c.453T>C (p.Phe151=) | |
12 | g.8059733A>T | CA383798907 | C3AR1 | c.453T>A (p.Phe151Leu) | |
12 | g.8059736del | CA232559536 | C3AR1 | c.453del (p.Phe151LeufsTer2) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.8059734A>C | CA383798908 | C3AR1 | c.452T>G (p.Phe151Cys) | |
12 | g.8059734A>G | CA383798909 | C3AR1 | c.452T>C (p.Phe151Ser) | |
12 | g.8059734A>T | CA383798910 | C3AR1 | c.452T>A (p.Phe151Tyr) | |
12 | g.8059735A= | CA2014849547 | C3AR1 | c.451T= (p.Phe151=) | |
12 | g.8059735A>C | CA383798912 | C3AR1 | c.451T>G (p.Phe151Val) | |
12 | g.8059735A>G | CA6432008 | C3AR1 | c.451T>C (p.Phe151Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.8059735A>T | CA383798911 | C3AR1 | c.451T>A (p.Phe151Ile) | |
12 | g.8059736A>C | CA478528891 | C3AR1 | c.450T>G (p.Ala150=) | |
12 | g.8059736A>G | CA478528894 | C3AR1 | c.450T>C (p.Ala150=) | |
12 | g.8059736A>T | CA478528893 | C3AR1 | c.450T>A (p.Ala150=) | |
12 | g.8059737G>A | CA383798914 | C3AR1 | c.449C>T (p.Ala150Val) | gnomAD v4 |
12 | g.8059737G>C | CA383798916 | C3AR1 | c.449C>G (p.Ala150Gly) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.8059737G= | CA2014849548 | C3AR1 | c.449C= (p.Ala150=) | |
12 | g.8059737G>T | CA383798918 | C3AR1 | c.449C>A (p.Ala150Asp) | ClinVar dbSNP |
12 | g.8059738C>A | CA383798919 | C3AR1 | c.448G>T (p.Ala150Ser) | |
12 | g.8059738C= | CA2014849549 | C3AR1 | c.448G= (p.Ala150=) | |
12 | g.8059738C>G | CA232559557 | C3AR1 | c.448G>C (p.Ala150Pro) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.8059738C>T | CA383798922 | C3AR1 | c.448G>A (p.Ala150Thr) | |
12 | g.8059739C>A | CA478528896 | C3AR1 | c.447G>T (p.Val149=) | |
12 | g.8059739C= | CA2014849550 | C3AR1 | c.447G= (p.Val149=) | |
12 | g.8059739C>G | CA478528897 | C3AR1 | c.447G>C (p.Val149=) | |
12 | g.8059739C>T | CA478528898 | C3AR1 | c.447G>A (p.Val149=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.8059740A>C | CA383798924 | C3AR1 | c.446T>G (p.Val149Gly) | |
12 | g.8059740A>G | CA383798926 | C3AR1 | c.446T>C (p.Val149Ala) | |
12 | g.8059740A>T | CA383798928 | C3AR1 | c.446T>A (p.Val149Glu) | |
12 | g.8059741C>A | CA383798930 | C3AR1 | c.445G>T (p.Val149Leu) | COSMIC |
12 | g.8059741C>G | CA383798932 | C3AR1 | c.445G>C (p.Val149Leu) | |
12 | g.8059741C>T | CA383798933 | C3AR1 | c.445G>A (p.Val149Met) | gnomAD v4 |
12 | g.8059742C>A | CA478528900 | C3AR1 | c.444G>T (p.Val148=) | dbSNP |
12 | g.8059742C= | CA2014849551 | C3AR1 | c.444G= (p.Val148=) | |
12 | g.8059742C>G | CA478528901 | C3AR1 | c.444G>C (p.Val148=) | |
12 | g.8059742C>T | CA478528903 | C3AR1 | c.444G>A (p.Val148=) | |
12 | g.8059743A= | CA2014849552 | C3AR1 | c.443T= (p.Val148=) | |
12 | g.8059743A>C | CA383798935 | C3AR1 | c.443T>G (p.Val148Gly) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.8059743A>G | CA383798937 | C3AR1 | c.443T>C (p.Val148Ala) | dbSNP gnomAD v4 |
12 | g.8059743A>T | CA383798934 | C3AR1 | c.443T>A (p.Val148Glu) | |
12 | g.8059744C>A | CA383798940 | C3AR1 | c.442G>T (p.Val148Leu) | |
12 | g.8059744C= | CA2014849553 | C3AR1 | c.442G= (p.Val148=) | |
12 | g.8059744C>G | CA383798941 | C3AR1 | c.442G>C (p.Val148Leu) | |
12 | g.8059744C>T | CA383798943 | C3AR1 | c.442G>A (p.Val148Met) | dbSNP gnomAD v4 |
12 | g.8059745C>A | CA383798945 | C3AR1 | c.441G>T (p.Trp147Cys) | |
12 | g.8059745C>G | CA383798947 | C3AR1 | c.441G>C (p.Trp147Cys) |