Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.154580323_154590216del | CA915940499 | |||
4 | g.154585993_154586004del | CA2578217778 | FGA | c.1434_1445del (p.Thr479_Val482del) c.644-285_644-274del (n.644-285_644-274del) | gnomAD v4 |
4 | g.154585991del | CA2578217779 | FGA | c.1440del (p.Glu481LysfsTer3) c.644-279del (n.644-279del) | |
4 | g.154585991T>A | CA126484 | FGA | c.1438A>T (p.Lys480Ter) c.644-281A>T (n.644-281A>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154585991T>C | CA358529042 | FGA | c.1438A>G (p.Lys480Glu) c.644-281A>G (n.644-281A>G) | gnomAD v4 |
4 | g.154585991T>G | CA358529044 | FGA | c.1438A>C (p.Lys480Gln) c.644-281A>C (n.644-281A>C) | |
4 | g.154585991T= | CA1504943287 | FGA | c.1438A= (p.Lys480=) c.644-281A= (n.644-281A=) | |
4 | g.154585992G>A | CA442014031 | FGA | c.1437C>T (p.Thr479=) c.644-282C>T (n.644-282C>T) | |
4 | g.154585992G>C | CA442014033 | FGA | c.1437C>G (p.Thr479=) c.644-282C>G (n.644-282C>G) | |
4 | g.154585992G>T | CA442014032 | FGA | c.1437C>A (p.Thr479=) c.644-282C>A (n.644-282C>A) | |
4 | g.154585993G>A | CA358529047 | FGA | c.1436C>T (p.Thr479Ile) c.644-283C>T (n.644-283C>T) | gnomAD v4 COSMIC COSMIC |
4 | g.154585993G>C | CA358529048 | FGA | c.1436C>G (p.Thr479Ser) c.644-283C>G (n.644-283C>G) | |
4 | g.154585993G>T | CA358529049 | FGA | c.1436C>A (p.Thr479Asn) c.644-283C>A (n.644-283C>A) | gnomAD v4 |
4 | g.154585994T>A | CA358529052 | FGA | c.1435A>T (p.Thr479Ser) c.644-284A>T (n.644-284A>T) | |
4 | g.154585994T>C | CA358529054 | FGA | c.1435A>G (p.Thr479Ala) c.644-284A>G (n.644-284A>G) | |
4 | g.154585994T>G | CA358529055 | FGA | c.1435A>C (p.Thr479Pro) c.644-284A>C (n.644-284A>C) | |
4 | g.154585995A>C | CA442014036 | FGA | c.1434T>G (p.Val478=) c.644-285T>G (n.644-285T>G) | |
4 | g.154585995A>G | CA442014037 | FGA | c.1434T>C (p.Val478=) c.644-285T>C (n.644-285T>C) | gnomAD v4 |
4 | g.154585995A>T | CA442014038 | FGA | c.1434T>A (p.Val478=) c.644-285T>A (n.644-285T>A) | |
4 | g.154585996A>C | CA358529058 | FGA | c.1433T>G (p.Val478Gly) c.644-286T>G (n.644-286T>G) | |
4 | g.154585996A>G | CA358529062 | FGA | c.1433T>C (p.Val478Ala) c.644-286T>C (n.644-286T>C) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.154585996A>T | CA358529060 | FGA | c.1433T>A (p.Val478Asp) c.644-286T>A (n.644-286T>A) | |
4 | g.154585997C>A | CA358529064 | FGA | c.1432G>T (p.Val478Phe) c.644-287G>T (n.644-287G>T) | |
4 | g.154585997C>G | CA358529066 | FGA | c.1432G>C (p.Val478Leu) c.644-287G>C (n.644-287G>C) | |
4 | g.154585997C>T | CA358529069 | FGA | c.1432G>A (p.Val478Ile) c.644-287G>A (n.644-287G>A) | |
4 | g.154585998T>A | CA358529071 | FGA | c.1431A>T (p.Glu477Asp) c.644-288A>T (n.644-288A>T) | |
4 | g.154585998T>C | CA442014040 | FGA | c.1431A>G (p.Glu477=) c.644-288A>G (n.644-288A>G) | |
4 | g.154585998T>G | CA358529073 | FGA | c.1431A>C (p.Glu477Asp) c.644-288A>C (n.644-288A>C) | |
4 | g.154585999T>A | CA358529076 | FGA | c.1430A>T (p.Glu477Val) c.644-289A>T (n.644-289A>T) | |
4 | g.154585999T>C | CA358529077 | FGA | c.1430A>G (p.Glu477Gly) c.644-289A>G (n.644-289A>G) | |
4 | g.154585999T>G | CA358529079 | FGA | c.1430A>C (p.Glu477Ala) c.644-289A>C (n.644-289A>C) | |
4 | g.154586000C>A | CA358529082 | FGA | c.1429G>T (p.Glu477Ter) c.644-290G>T (n.644-290G>T) | COSMIC COSMIC |
4 | g.154586000C= | CA1504943288 | FGA | c.1429G= (p.Glu477=) c.644-290G= (n.644-290G=) | |
4 | g.154586000C>G | CA358529083 | FGA | c.1429G>C (p.Glu477Gln) c.644-290G>C (n.644-290G>C) | dbSNP |
4 | g.154586000C>T | CA358529085 | FGA | c.1429G>A (p.Glu477Lys) c.644-290G>A (n.644-290G>A) | |
4 | g.154586001T>A | CA358529087 | FGA | c.1428A>T (p.Lys476Asn) c.644-291A>T (n.644-291A>T) | |
4 | g.154586001T>C | CA442014043 | FGA | c.1428A>G (p.Lys476=) c.644-291A>G (n.644-291A>G) | |
4 | g.154586001T>G | CA358529090 | FGA | c.1428A>C (p.Lys476Asn) c.644-291A>C (n.644-291A>C) | |
4 | g.154586002T>A | CA358529093 | FGA | c.1427A>T (p.Lys476Ile) c.644-292A>T (n.644-292A>T) | |
4 | g.154586002T>C | CA108761169 | FGA | c.1427A>G (p.Lys476Arg) c.644-292A>G (n.644-292A>G) | dbSNP |
4 | g.154586002T>G | CA358529095 | FGA | c.1427A>C (p.Lys476Thr) c.644-292A>C (n.644-292A>C) | |
4 | g.154586002T= | CA1504943289 | FGA | c.1427A= (p.Lys476=) c.644-292A= (n.644-292A=) | |
4 | g.154586003T>A | CA358529100 | FGA | c.1426A>T (p.Lys476Ter) c.644-293A>T (n.644-293A>T) | |
4 | g.154586003T>C | CA358529101 | FGA | c.1426A>G (p.Lys476Glu) c.644-293A>G (n.644-293A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154586003T>G | CA358529103 | FGA | c.1426A>C (p.Lys476Gln) c.644-293A>C (n.644-293A>C) | |
4 | g.154586003T= | CA1504943290 | FGA | c.1426A= (p.Lys476=) c.644-293A= (n.644-293A=) | |
4 | g.154586004G>A | CA442014045 | FGA | c.1425C>T (p.His475=) c.644-294C>T (n.644-294C>T) | |
4 | g.154586004G>C | CA358529105 | FGA | c.1425C>G (p.His475Gln) c.644-294C>G (n.644-294C>G) | dbSNP gnomAD v4 |
4 | g.154586004G= | CA1504943291 | FGA | c.1425C= (p.His475=) c.644-294C= (n.644-294C=) | |
4 | g.154586004G>T | CA358529107 | FGA | c.1425C>A (p.His475Gln) c.644-294C>A (n.644-294C>A) |