Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.132892310G>A | CA3408914 | AFF4 | c.2491C>T (p.Arg831Trp) c.1357C>T (p.Arg453Trp) c.2404C>T (p.Arg802Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.132892310G>C | CA360929176 | AFF4 | c.2491C>G (p.Arg831Gly) c.1357C>G (p.Arg453Gly) c.2404C>G (p.Arg802Gly) | COSMIC |
5 | g.132892310G= | CA1583372507 | AFF4 | c.2491C= (p.Arg831=) c.1357C= (p.Arg453=) c.2404C= (p.Arg802=) | |
5 | g.132892310G>T | CA446498901 | AFF4 | c.2491C>A (p.Arg831=) c.1357C>A (p.Arg453=) c.2404C>A (p.Arg802=) | |
5 | g.132892311A>C | CA446498902 | AFF4 | c.2490T>G (p.Ser830=) c.1356T>G (p.Ser452=) c.2403T>G (p.Ser801=) | |
5 | g.132892311A>G | CA446498903 | AFF4 | c.2490T>C (p.Ser830=) c.1356T>C (p.Ser452=) c.2403T>C (p.Ser801=) | |
5 | g.132892311A>T | CA446498904 | AFF4 | c.2490T>A (p.Ser830=) c.1356T>A (p.Ser452=) c.2403T>A (p.Ser801=) | |
5 | g.132892312G>A | CA360929178 | AFF4 | c.2489C>T (p.Ser830Phe) c.1355C>T (p.Ser452Phe) c.2402C>T (p.Ser801Phe) | gnomAD v4 |
5 | g.132892312G>C | CA360929180 | AFF4 | c.2489C>G (p.Ser830Cys) c.1355C>G (p.Ser452Cys) c.2402C>G (p.Ser801Cys) | gnomAD v4 |
5 | g.132892312G>T | CA360929182 | AFF4 | c.2489C>A (p.Ser830Tyr) c.1355C>A (p.Ser452Tyr) c.2402C>A (p.Ser801Tyr) | |
5 | g.132892313A>C | CA360929183 | AFF4 | c.2488T>G (p.Ser830Ala) c.1354T>G (p.Ser452Ala) c.2401T>G (p.Ser801Ala) | |
5 | g.132892313A>G | CA360929184 | AFF4 | c.2488T>C (p.Ser830Pro) c.1354T>C (p.Ser452Pro) c.2401T>C (p.Ser801Pro) | |
5 | g.132892313A>T | CA360929185 | AFF4 | c.2488T>A (p.Ser830Thr) c.1354T>A (p.Ser452Thr) c.2401T>A (p.Ser801Thr) | |
5 | g.132892314G>A | CA446498905 | AFF4 | c.2487C>T (p.Gly829=) c.1353C>T (p.Gly451=) c.2400C>T (p.Gly800=) | gnomAD v4 |
5 | g.132892314G>C | CA446498906 | AFF4 | c.2487C>G (p.Gly829=) c.1353C>G (p.Gly451=) c.2400C>G (p.Gly800=) | |
5 | g.132892314G>T | CA446498907 | AFF4 | c.2487C>A (p.Gly829=) c.1353C>A (p.Gly451=) c.2400C>A (p.Gly800=) | |
5 | g.132892315C>A | CA360929188 | AFF4 | c.2486G>T (p.Gly829Val) c.1352G>T (p.Gly451Val) c.2399G>T (p.Gly800Val) | |
5 | g.132892315C= | CA1583372508 | AFF4 | c.2486G= (p.Gly829=) c.1352G= (p.Gly451=) c.2399G= (p.Gly800=) | |
5 | g.132892315C>G | CA127270212 | AFF4 | c.2486G>C (p.Gly829Ala) c.1352G>C (p.Gly451Ala) c.2399G>C (p.Gly800Ala) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.132892315C>T | CA360929186 | AFF4 | c.2486G>A (p.Gly829Asp) c.1352G>A (p.Gly451Asp) c.2399G>A (p.Gly800Asp) | |
5 | g.132892316C>A | CA360929191 | AFF4 | c.2485G>T (p.Gly829Cys) c.1351G>T (p.Gly451Cys) c.2398G>T (p.Gly800Cys) | |
5 | g.132892316C= | CA1583372509 | AFF4 | c.2485G= (p.Gly829=) c.1351G= (p.Gly451=) c.2398G= (p.Gly800=) | |
5 | g.132892316C>G | CA360929193 | AFF4 | c.2485G>C (p.Gly829Arg) c.1351G>C (p.Gly451Arg) c.2398G>C (p.Gly800Arg) | ClinVar dbSNP gnomAD v4 |
5 | g.132892316C>T | CA3408915 | AFF4 | c.2485G>A (p.Gly829Ser) c.1351G>A (p.Gly451Ser) c.2398G>A (p.Gly800Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.132892317A>C | CA360929196 | AFF4 | c.2484T>G (p.His828Gln) c.1350T>G (p.His450Gln) c.2397T>G (p.His799Gln) | |
5 | g.132892317A>G | CA446498908 | AFF4 | c.2484T>C (p.His828=) c.1350T>C (p.His450=) c.2397T>C (p.His799=) | |
5 | g.132892317A>T | CA360929198 | AFF4 | c.2484T>A (p.His828Gln) c.1350T>A (p.His450Gln) c.2397T>A (p.His799Gln) | |
5 | g.132892318T>A | CA360929203 | AFF4 | c.2483A>T (p.His828Leu) c.1349A>T (p.His450Leu) c.2396A>T (p.His799Leu) | |
5 | g.132892318T>C | CA360929200 | AFF4 | c.2483A>G (p.His828Arg) c.1349A>G (p.His450Arg) c.2396A>G (p.His799Arg) | dbSNP gnomAD v4 |
5 | g.132892318T>G | CA360929201 | AFF4 | c.2483A>C (p.His828Pro) c.1349A>C (p.His450Pro) c.2396A>C (p.His799Pro) | |
5 | g.132892318T= | CA1583372510 | AFF4 | c.2483A= (p.His828=) c.1349A= (p.His450=) c.2396A= (p.His799=) | |
5 | g.132892319G>A | CA360929205 | AFF4 | c.2482C>T (p.His828Tyr) c.1348C>T (p.His450Tyr) c.2395C>T (p.His799Tyr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
5 | g.132892319G>C | CA360929208 | AFF4 | c.2482C>G (p.His828Asp) c.1348C>G (p.His450Asp) c.2395C>G (p.His799Asp) | |
5 | g.132892319G= | CA1583372511 | AFF4 | c.2482C= (p.His828=) c.1348C= (p.His450=) c.2395C= (p.His799=) | |
5 | g.132892319G>T | CA360929210 | AFF4 | c.2482C>A (p.His828Asn) c.1348C>A (p.His450Asn) c.2395C>A (p.His799Asn) | dbSNP |
5 | g.132892320C>A | CA360929211 | AFF4 | c.2481G>T (p.Glu827Asp) c.1347G>T (p.Glu449Asp) c.2394G>T (p.Glu798Asp) | |
5 | g.132892320C>G | CA360929212 | AFF4 | c.2481G>C (p.Glu827Asp) c.1347G>C (p.Glu449Asp) c.2394G>C (p.Glu798Asp) | |
5 | g.132892320C>T | CA446498909 | AFF4 | c.2481G>A (p.Glu827=) c.1347G>A (p.Glu449=) c.2394G>A (p.Glu798=) | |
5 | g.132892321T>A | CA360929215 | AFF4 | c.2480A>T (p.Glu827Val) c.1346A>T (p.Glu449Val) c.2393A>T (p.Glu798Val) | |
5 | g.132892321T>C | CA360929219 | AFF4 | c.2480A>G (p.Glu827Gly) c.1346A>G (p.Glu449Gly) c.2393A>G (p.Glu798Gly) | gnomAD v4 |
5 | g.132892321T>G | CA360929217 | AFF4 | c.2480A>C (p.Glu827Ala) c.1346A>C (p.Glu449Ala) c.2393A>C (p.Glu798Ala) | |
5 | g.132892322C>A | CA360929221 | AFF4 | c.2479G>T (p.Glu827Ter) c.1345G>T (p.Glu449Ter) c.2392G>T (p.Glu798Ter) | |
5 | g.132892322C>G | CA360929223 | AFF4 | c.2479G>C (p.Glu827Gln) c.1345G>C (p.Glu449Gln) c.2392G>C (p.Glu798Gln) | |
5 | g.132892322C>T | CA360929225 | AFF4 | c.2479G>A (p.Glu827Lys) c.1345G>A (p.Glu449Lys) c.2392G>A (p.Glu798Lys) | |
5 | g.132892323T>A | CA446498910 | AFF4 | c.2478A>T (p.Thr826=) c.1344A>T (p.Thr448=) c.2391A>T (p.Thr797=) | |
5 | g.132892323T>C | CA446498912 | AFF4 | c.2478A>G (p.Thr826=) c.1344A>G (p.Thr448=) c.2391A>G (p.Thr797=) | |
5 | g.132892323T>G | CA446498911 | AFF4 | c.2478A>C (p.Thr826=) c.1344A>C (p.Thr448=) c.2391A>C (p.Thr797=) | |
5 | g.132892324G>A | CA360929226 | AFF4 | c.2477C>T (p.Thr826Ile) c.1343C>T (p.Thr448Ile) c.2390C>T (p.Thr797Ile) | gnomAD v4 |
5 | g.132892324G>C | CA360929228 | AFF4 | c.2477C>G (p.Thr826Arg) c.1343C>G (p.Thr448Arg) c.2390C>G (p.Thr797Arg) | |
5 | g.132892324G>T | CA360929229 | AFF4 | c.2477C>A (p.Thr826Lys) c.1343C>A (p.Thr448Lys) c.2390C>A (p.Thr797Lys) |