Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.49130334A= | CA1363342483 | LAMB2 | c.1122T= (p.Cys374=) | |
3 | g.49130334A>C | CA352743323 | LAMB2 | c.1122T>G (p.Cys374Trp) | |
3 | g.49130334A>G | CA433835438 | LAMB2 | c.1122T>C (p.Cys374=) | |
3 | g.49130334A>T | CA124110 | LAMB2 | c.1122T>A (p.Cys374Ter) | ClinVar dbSNP gnomAD v4 |
3 | g.49130335C>A | CA352743327 | LAMB2 | c.1121G>T (p.Cys374Phe) | |
3 | g.49130335C= | CA1363342484 | LAMB2 | c.1121G= (p.Cys374=) | |
3 | g.49130335C>G | CA352743329 | LAMB2 | c.1121G>C (p.Cys374Ser) | |
3 | g.49130335C>T | CA352743331 | LAMB2 | c.1121G>A (p.Cys374Tyr) | dbSNP |
3 | g.49130336A= | CA1363342485 | LAMB2 | c.1120T= (p.Cys374=) | |
3 | g.49130336A>C | CA352743333 | LAMB2 | c.1120T>G (p.Cys374Gly) | |
3 | g.49130336A>G | CA2394687 | LAMB2 | c.1120T>C (p.Cys374Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.49130336A>T | CA352743336 | LAMB2 | c.1120T>A (p.Cys374Ser) | |
3 | g.49130337C>A | CA433835456 | LAMB2 | c.1119G>T (p.Val373=) | |
3 | g.49130337C>G | CA433835458 | LAMB2 | c.1119G>C (p.Val373=) | |
3 | g.49130337C>T | CA433835460 | LAMB2 | c.1119G>A (p.Val373=) | gnomAD v4 |
3 | g.49130338A= | CA1363342486 | LAMB2 | c.1118T= (p.Val373=) | |
3 | g.49130338A>C | CA352743341 | LAMB2 | c.1118T>G (p.Val373Gly) | |
3 | g.49130338A>G | CA352743343 | LAMB2 | c.1118T>C (p.Val373Ala) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.49130338A>T | CA352743346 | LAMB2 | c.1118T>A (p.Val373Glu) | |
3 | g.49130339C>A | CA352743349 | LAMB2 | c.1117G>T (p.Val373Leu) | |
3 | g.49130339C>G | CA352743350 | LAMB2 | c.1117G>C (p.Val373Leu) | |
3 | g.49130339C>T | CA352743353 | LAMB2 | c.1117G>A (p.Val373Met) | ClinVar gnomAD v4 |
3 | g.49130340A>C | CA433835468 | LAMB2 | c.1116T>G (p.Gly372=) | |
3 | g.49130340A>G | CA433835467 | LAMB2 | c.1116T>C (p.Gly372=) | |
3 | g.49130340A>T | CA433835465 | LAMB2 | c.1116T>A (p.Gly372=) | |
3 | g.49130341C>A | CA352743363 | LAMB2 | c.1115G>T (p.Gly372Val) | |
3 | g.49130341C>G | CA352743361 | LAMB2 | c.1115G>C (p.Gly372Ala) | |
3 | g.49130341C>T | CA352743358 | LAMB2 | c.1115G>A (p.Gly372Asp) | |
3 | g.49130342C>A | CA352743367 | LAMB2 | c.1114G>T (p.Gly372Cys) | |
3 | g.49130342C>G | CA352743371 | LAMB2 | c.1114G>C (p.Gly372Arg) | |
3 | g.49130342C>T | CA352743369 | LAMB2 | c.1114G>A (p.Gly372Ser) | |
3 | g.49130343T>A | CA433835478 | LAMB2 | c.1113A>T (p.Gly371=) | |
3 | g.49130343T>C | CA433835481 | LAMB2 | c.1113A>G (p.Gly371=) | dbSNP |
3 | g.49130343T>G | CA433835483 | LAMB2 | c.1113A>C (p.Gly371=) | |
3 | g.49130343T= | CA1363342487 | LAMB2 | c.1113A= (p.Gly371=) | |
3 | g.49130344C>A | CA352743375 | LAMB2 | c.1112G>T (p.Gly371Val) | |
3 | g.49130344C= | CA1363342488 | LAMB2 | c.1112G= (p.Gly371=) | |
3 | g.49130344C>G | CA352743378 | LAMB2 | c.1112G>C (p.Gly371Ala) | dbSNP |
3 | g.49130344C>T | CA352743381 | LAMB2 | c.1112G>A (p.Gly371Glu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
3 | g.49130345C>A | CA352743384 | LAMB2 | c.1111G>T (p.Gly371Ter) | |
3 | g.49130345C>G | CA352743387 | LAMB2 | c.1111G>C (p.Gly371Arg) | |
3 | g.49130345C>T | CA352743389 | LAMB2 | c.1111G>A (p.Gly371Arg) | |
3 | g.49130346A= | CA1363342489 | LAMB2 | c.1110T= (p.Ser370=) | |
3 | g.49130346A>C | CA352743392 | LAMB2 | c.1110T>G (p.Ser370Arg) | |
3 | g.49130346A>G | CA433835497 | LAMB2 | c.1110T>C (p.Ser370=) | |
3 | g.49130346A>T | CA74487490 | LAMB2 | c.1110T>A (p.Ser370Arg) | dbSNP |
3 | g.49130347C>A | CA352743396 | LAMB2 | c.1109G>T (p.Ser370Ile) | |
3 | g.49130347C>G | CA352743399 | LAMB2 | c.1109G>C (p.Ser370Thr) | |
3 | g.49130347C>T | CA352743402 | LAMB2 | c.1109G>A (p.Ser370Asn) | |
3 | g.49130348T>A | CA352743411 | LAMB2 | c.1108A>T (p.Ser370Cys) |