Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.25245298del | CA891842141 | KRAS | c.88del (p.Asp30ThrfsTer7) c.-88+5454del (n.-88+5454del) | |
12 | g.25245298C>A | CA478891779 | KRAS | c.87G>T (p.Val29=) c.-88+5453G>T (n.-88+5453G>T) | gnomAD v4 |
12 | g.25245298C>G | CA478891781 | KRAS | c.87G>C (p.Val29=) c.-88+5453G>C (n.-88+5453G>C) | |
12 | g.25245298C>T | CA478891782 | KRAS | c.87G>A (p.Val29=) c.-88+5453G>A (n.-88+5453G>A) | dbSNP |
12 | g.25245299A>C | CA384157295 | KRAS | c.86T>G (p.Val29Gly) c.-88+5452T>G (n.-88+5452T>G) | |
12 | g.25245299A>G | CA384157292 | KRAS | c.86T>C (p.Val29Ala) c.-88+5452T>C (n.-88+5452T>C) | |
12 | g.25245299A>T | CA384157294 | KRAS | c.86T>A (p.Val29Glu) c.-88+5452T>A (n.-88+5452T>A) | dbSNP |
12 | g.25245300C>A | CA384157297 | KRAS | c.85G>T (p.Val29Leu) c.-88+5451G>T (n.-88+5451G>T) | |
12 | g.25245300C>G | CA384157298 | KRAS | c.85G>C (p.Val29Leu) c.-88+5451G>C (n.-88+5451G>C) | |
12 | g.25245300C>T | CA384157299 | KRAS | c.85G>A (p.Val29Met) c.-88+5451G>A (n.-88+5451G>A) | |
12 | g.25245301A>C | CA384157301 | KRAS | c.84T>G (p.Phe28Leu) c.-88+5450T>G (n.-88+5450T>G) | |
12 | g.25245301A>G | CA478891792 | KRAS | c.84T>C (p.Phe28=) c.-88+5450T>C (n.-88+5450T>C) | |
12 | g.25245301A>T | CA384157303 | KRAS | c.84T>A (p.Phe28Leu) c.-88+5450T>A (n.-88+5450T>A) | ClinVar |
12 | g.25245304del | CA2580085329 | KRAS | c.84del (p.Phe28LeufsTer9) c.-88+5450del (n.-88+5450del) | ClinVar gnomAD v4 |
12 | g.25245302A>C | CA384157304 | KRAS | c.83T>G (p.Phe28Cys) c.-88+5449T>G (n.-88+5449T>G) | |
12 | g.25245302A>G | CA384157306 | KRAS | c.83T>C (p.Phe28Ser) c.-88+5449T>C (n.-88+5449T>C) | COSMIC |
12 | g.25245302A>T | CA384157305 | KRAS | c.83T>A (p.Phe28Tyr) c.-88+5449T>A (n.-88+5449T>A) | |
12 | g.25245303A>C | CA384157308 | KRAS | c.82T>G (p.Phe28Val) c.-88+5448T>G (n.-88+5448T>G) | |
12 | g.25245303A>G | CA384157310 | KRAS | c.82T>C (p.Phe28Leu) c.-88+5448T>C (n.-88+5448T>C) | |
12 | g.25245303A>T | CA384157311 | KRAS | c.82T>A (p.Phe28Ile) c.-88+5448T>A (n.-88+5448T>A) | |
12 | g.25245304A>C | CA384157313 | KRAS | c.81T>G (p.His27Gln) c.-88+5447T>G (n.-88+5447T>G) | |
12 | g.25245304A>G | CA478891803 | KRAS | c.81T>C (p.His27=) c.-88+5447T>C (n.-88+5447T>C) | gnomAD v4 |
12 | g.25245304A>T | CA384157314 | KRAS | c.81T>A (p.His27Gln) c.-88+5447T>A (n.-88+5447T>A) | |
12 | g.25245305T>A | CA384157316 | KRAS | c.80A>T (p.His27Leu) c.-88+5446A>T (n.-88+5446A>T) | ClinVar dbSNP COSMIC |
12 | g.25245305T>C | CA384157317 | KRAS | c.80A>G (p.His27Arg) c.-88+5446A>G (n.-88+5446A>G) | ClinVar |
12 | g.25245305T>G | CA384157318 | KRAS | c.80A>C (p.His27Pro) c.-88+5446A>C (n.-88+5446A>C) | |
12 | g.25245308_25245313del | CA2499221594 | KRAS | c.75_80del (p.Gln25_Asn26del) c.-88+5441_-88+5446del (n.-88+5441_-88+5446del) | ClinVar dbSNP |
12 | g.25245306G>A | CA384157320 | KRAS | c.79C>T (p.His27Tyr) c.-88+5445C>T (n.-88+5445C>T) | dbSNP COSMIC |
12 | g.25245306G>C | CA384157321 | KRAS | c.79C>G (p.His27Asp) c.-88+5445C>G (n.-88+5445C>G) | dbSNP |
12 | g.25245306G>T | CA384157323 | KRAS | c.79C>A (p.His27Asn) c.-88+5445C>A (n.-88+5445C>A) | |
12 | g.25245307A>C | CA384157325 | KRAS | c.78T>G (p.Asn26Lys) c.-88+5444T>G (n.-88+5444T>G) | |
12 | g.25245307A>G | CA478891809 | KRAS | c.78T>C (p.Asn26=) c.-88+5444T>C (n.-88+5444T>C) | |
12 | g.25245307A>T | CA384157324 | KRAS | c.78T>A (p.Asn26Lys) c.-88+5444T>A (n.-88+5444T>A) | dbSNP |
12 | g.25245308T>A | CA384157326 | KRAS | c.77A>T (p.Asn26Ile) c.-88+5443A>T (n.-88+5443A>T) | dbSNP |
12 | g.25245308T>C | CA384157330 | KRAS | c.77A>G (p.Asn26Ser) c.-88+5443A>G (n.-88+5443A>G) | |
12 | g.25245308T>G | CA384157328 | KRAS | c.77A>C (p.Asn26Thr) c.-88+5443A>C (n.-88+5443A>C) | ClinVar |
12 | g.25245309T>A | CA241569 | KRAS | c.76A>T (p.Asn26Tyr) c.-88+5442A>T (n.-88+5442A>T) | ClinVar dbSNP gnomAD v4 |
12 | g.25245309T>C | CA384157333 | KRAS | c.76A>G (p.Asn26Asp) c.-88+5442A>G (n.-88+5442A>G) | |
12 | g.25245309T>G | CA384157332 | KRAS | c.76A>C (p.Asn26His) c.-88+5442A>C (n.-88+5442A>C) | ClinVar dbSNP |
12 | g.25245309T= | CA2022898184 | KRAS | c.76A= (p.Asn26=) c.-88+5442A= (n.-88+5442A=) | |
12 | g.25245309_25245310insA | CA645572102 | KRAS | c.75_76insT (p.Asn26Ter) c.-88+5441_-88+5442insT (n.-88+5441_-88+5442insT) | COSMIC COSMIC |
12 | g.25245310C>A | CA384157335 | KRAS | c.75G>T (p.Gln25His) c.-88+5441G>T (n.-88+5441G>T) | |
12 | g.25245310C>G | CA384157337 | KRAS | c.75G>C (p.Gln25His) c.-88+5441G>C (n.-88+5441G>C) | dbSNP |
12 | g.25245310C>T | CA478891821 | KRAS | c.75G>A (p.Gln25=) c.-88+5441G>A (n.-88+5441G>A) | ClinVar dbSNP |
12 | g.25245311T>A | CA384157339 | KRAS | c.74A>T (p.Gln25Leu) c.-88+5440A>T (n.-88+5440A>T) | ClinVar |
12 | g.25245311T>C | CA384157340 | KRAS | c.74A>G (p.Gln25Arg) c.-88+5440A>G (n.-88+5440A>G) | ClinVar dbSNP gnomAD v4 |
12 | g.25245311T>G | CA384157342 | KRAS | c.74A>C (p.Gln25Pro) c.-88+5440A>C (n.-88+5440A>C) | |
12 | g.25245312G>A | CA384157344 | KRAS | c.73C>T (p.Gln25Ter) c.-88+5439C>T (n.-88+5439C>T) | dbSNP |
12 | g.25245312G>C | CA384157345 | KRAS | c.73C>G (p.Gln25Glu) c.-88+5439C>G (n.-88+5439C>G) | dbSNP |
12 | g.25245312G= | CA2022898196 | KRAS | c.73C= (p.Gln25=) c.-88+5439C= (n.-88+5439C=) |