Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.73442256T>A | CA1468178450 | AFP | c.483-40T>A (n.483-40T>A) c.480-40T>A (n.480-40T>A) c.9-40T>A (n.9-40T>A) | dbSNP |
4 | g.73442256T>C | CA2670968480 | AFP | c.483-40T>C (n.483-40T>C) c.480-40T>C (n.480-40T>C) c.9-40T>C (n.9-40T>C) | gnomAD v4 |
4 | g.73442256T= | CA1468178449 | AFP | c.483-40T= (n.483-40T=) c.480-40T= (n.480-40T=) c.9-40T= (n.9-40T=) | |
4 | g.73442257A>T | CA2578111920 | AFP | c.483-39A>T (n.483-39A>T) c.480-39A>T (n.480-39A>T) c.9-39A>T (n.9-39A>T) | |
4 | g.73442258G>A | CA1064122145 | AFP | c.483-38G>A (n.483-38G>A) c.480-38G>A (n.480-38G>A) c.9-38G>A (n.9-38G>A) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.73442258G= | CA1468178452 | AFP | c.483-38G= (n.483-38G=) c.480-38G= (n.480-38G=) c.9-38G= (n.9-38G=) | |
4 | g.73442259G>A | CA2670968482 | AFP | c.483-37G>A (n.483-37G>A) c.480-37G>A (n.480-37G>A) c.9-37G>A (n.9-37G>A) | gnomAD v4 |
4 | g.73442259G= | CA1468178456 | AFP | c.483-37G= (n.483-37G=) c.480-37G= (n.480-37G=) c.9-37G= (n.9-37G=) | |
4 | g.73442259G>T | CA552303740 | AFP | c.483-37G>T (n.483-37G>T) c.480-37G>T (n.480-37G>T) c.9-37G>T (n.9-37G>T) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.73442260T>A | CA2670968483 | AFP | c.483-36T>A (n.483-36T>A) c.480-36T>A (n.480-36T>A) c.9-36T>A (n.9-36T>A) | gnomAD v4 |
4 | g.73442260T>C | CA552303741 | AFP | c.483-36T>C (n.483-36T>C) c.480-36T>C (n.480-36T>C) c.9-36T>C (n.9-36T>C) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.73442260T= | CA1468178459 | AFP | c.483-36T= (n.483-36T=) c.480-36T= (n.480-36T=) c.9-36T= (n.9-36T=) | |
4 | g.73442261G>T | CA2670968485 | AFP | c.483-35G>T (n.483-35G>T) c.480-35G>T (n.480-35G>T) c.9-35G>T (n.9-35G>T) | gnomAD v4 |
4 | g.73442263T>C | CA2959930 | AFP | c.483-33T>C (n.483-33T>C) c.480-33T>C (n.480-33T>C) c.9-33T>C (n.9-33T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.73442263T= | CA1468178463 | AFP | c.483-33T= (n.483-33T=) c.480-33T= (n.480-33T=) c.9-33T= (n.9-33T=) | |
4 | g.73442265A= | CA1468178467 | AFP | c.483-31A= (n.483-31A=) c.480-31A= (n.480-31A=) c.9-31A= (n.9-31A=) | |
4 | g.73442265A>G | CA2959931 | AFP | c.483-31A>G (n.483-31A>G) c.480-31A>G (n.480-31A>G) c.9-31A>G (n.9-31A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.73442267A>T | CA2578111921 | AFP | c.483-29A>T (n.483-29A>T) c.480-29A>T (n.480-29A>T) c.9-29A>T (n.9-29A>T) | gnomAD v4 |
4 | g.73442270T>A | CA2959932 | AFP | c.483-26T>A (n.483-26T>A) c.480-26T>A (n.480-26T>A) c.9-26T>A (n.9-26T>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442270T>C | CA2670968489 | AFP | c.483-26T>C (n.483-26T>C) c.480-26T>C (n.480-26T>C) c.9-26T>C (n.9-26T>C) | gnomAD v4 |
4 | g.73442270T= | CA1468178469 | AFP | c.483-26T= (n.483-26T=) c.480-26T= (n.480-26T=) c.9-26T= (n.9-26T=) | |
4 | g.73442271C>A | CA2670968490 | AFP | c.483-25C>A (n.483-25C>A) c.480-25C>A (n.480-25C>A) c.9-25C>A (n.9-25C>A) | gnomAD v4 |
4 | g.73442272T>C | CA2578111922 | AFP | c.483-24T>C (n.483-24T>C) c.480-24T>C (n.480-24T>C) c.9-24T>C (n.9-24T>C) | gnomAD v4 |
4 | g.73442273T>A | CA552303742 | AFP | c.483-23T>A (n.483-23T>A) c.480-23T>A (n.480-23T>A) c.9-23T>A (n.9-23T>A) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.73442273T= | CA1468178471 | AFP | c.483-23T= (n.483-23T=) c.480-23T= (n.480-23T=) c.9-23T= (n.9-23T=) | |
4 | g.73442275T>C | CA2959933 | AFP | c.483-21T>C (n.483-21T>C) c.480-21T>C (n.480-21T>C) c.9-21T>C (n.9-21T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442275T= | CA1468178476 | AFP | c.483-21T= (n.483-21T=) c.480-21T= (n.480-21T=) c.9-21T= (n.9-21T=) | |
4 | g.73442276A>G | CA2670968492 | AFP | c.483-20A>G (n.483-20A>G) c.480-20A>G (n.480-20A>G) c.9-20A>G (n.9-20A>G) | gnomAD v4 |
4 | g.73442277G>C | CA2959934 | AFP | c.483-19G>C (n.483-19G>C) c.480-19G>C (n.480-19G>C) c.9-19G>C (n.9-19G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442277G= | CA1468178480 | AFP | c.483-19G= (n.483-19G=) c.480-19G= (n.480-19G=) c.9-19G= (n.9-19G=) | |
4 | g.73442277G>T | CA2670968494 | AFP | c.483-19G>T (n.483-19G>T) c.480-19G>T (n.480-19G>T) c.9-19G>T (n.9-19G>T) | gnomAD v4 |
4 | g.73442278C= | CA1468178485 | AFP | c.483-18C= (n.483-18C=) c.480-18C= (n.480-18C=) c.9-18C= (n.9-18C=) | |
4 | g.73442278C>G | CA99671527 | AFP | c.483-18C>G (n.483-18C>G) c.480-18C>G (n.480-18C>G) c.9-18C>G (n.9-18C>G) | dbSNP |
4 | g.73442278C>T | CA552303744 | AFP | c.483-18C>T (n.483-18C>T) c.480-18C>T (n.480-18C>T) c.9-18C>T (n.9-18C>T) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.73442279T>C | CA2762178478 | AFP | c.483-17T>C (n.483-17T>C) c.480-17T>C (n.480-17T>C) c.9-17T>C (n.9-17T>C) | |
4 | g.73442282A>G | CA2670968497 | AFP | c.483-14A>G (n.483-14A>G) c.480-14A>G (n.480-14A>G) c.9-14A>G (n.9-14A>G) | gnomAD v4 |
4 | g.73442286T>G | CA99671530 | AFP | c.483-10T>G (n.483-10T>G) c.480-10T>G (n.480-10T>G) c.9-10T>G (n.9-10T>G) | dbSNP |
4 | g.73442286T= | CA1468178488 | AFP | c.483-10T= (n.483-10T=) c.480-10T= (n.480-10T=) c.9-10T= (n.9-10T=) | |
4 | g.73442289T>C | CA2959935 | AFP | c.483-7T>C (n.483-7T>C) c.480-7T>C (n.480-7T>C) c.9-7T>C (n.9-7T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442289T= | CA1468178492 | AFP | c.483-7T= (n.483-7T=) c.480-7T= (n.480-7T=) c.9-7T= (n.9-7T=) | |
4 | g.73442290T>G | CA2959936 | AFP | c.483-6T>G (n.483-6T>G) c.480-6T>G (n.480-6T>G) c.9-6T>G (n.9-6T>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442290T= | CA1468178497 | AFP | c.483-6T= (n.483-6T=) c.480-6T= (n.480-6T=) c.9-6T= (n.9-6T=) | |
4 | g.73442291C>A | CA2670968498 | AFP | c.483-5C>A (n.483-5C>A) c.480-5C>A (n.480-5C>A) c.9-5C>A (n.9-5C>A) | gnomAD v4 |
4 | g.73442293C>T | CA2578111923 | AFP | c.483-3C>T (n.483-3C>T) c.480-3C>T (n.480-3C>T) c.9-3C>T (n.9-3C>T) | gnomAD v4 |
4 | g.73442294A>C | CA357236365 | AFP | c.483-2A>C (n.483-2A>C) c.480-2A>C (n.480-2A>C) c.9-2A>C (n.9-2A>C) | |
4 | g.73442294A>G | CA357236362 | AFP | c.483-2A>G (n.483-2A>G) c.480-2A>G (n.480-2A>G) c.9-2A>G (n.9-2A>G) | |
4 | g.73442294A>T | CA357236363 | AFP | c.483-2A>T (n.483-2A>T) c.480-2A>T (n.480-2A>T) c.9-2A>T (n.9-2A>T) | |
4 | g.73442295G>A | CA357236368 | AFP | c.483-1G>A (n.483-1G>A) c.480-1G>A (n.480-1G>A) c.9-1G>A (n.9-1G>A) | |
4 | g.73442295G>C | CA357236369 | AFP | c.483-1G>C (n.483-1G>C) c.480-1G>C (n.480-1G>C) c.9-1G>C (n.9-1G>C) | |
4 | g.73442295G>T | CA357236372 | AFP | c.483-1G>T (n.483-1G>T) c.480-1G>T (n.480-1G>T) c.9-1G>T (n.9-1G>T) | |
4 | g.73442296A>C | CA357236374 | AFP | c.483A>C (p.Lys161Asn) c.480A>C (p.Lys160Asn) c.9A>C (p.Lys3Asn) | |
4 | g.73442296A>G | CA439800122 | AFP | c.483A>G (p.Lys161=) c.480A>G (p.Lys160=) c.9A>G (p.Lys3=) | |
4 | g.73442296A>T | CA357236376 | AFP | c.483A>T (p.Lys161Asn) c.480A>T (p.Lys160Asn) c.9A>T (p.Lys3Asn) | |
4 | g.73442297T>A | CA357236379 | AFP | c.484T>A (p.Phe162Ile) c.481T>A (p.Phe161Ile) c.10T>A (p.Phe4Ile) | |
4 | g.73442297T>C | CA357236380 | AFP | c.484T>C (p.Phe162Leu) c.481T>C (p.Phe161Leu) c.10T>C (p.Phe4Leu) | gnomAD v4 |
4 | g.73442297T>G | CA357236383 | AFP | c.484T>G (p.Phe162Val) c.481T>G (p.Phe161Val) c.10T>G (p.Phe4Val) | |
4 | g.73442298T>A | CA357236385 | AFP | c.485T>A (p.Phe162Tyr) c.482T>A (p.Phe161Tyr) c.11T>A (p.Phe4Tyr) | |
4 | g.73442298T>C | CA357236386 | AFP | c.485T>C (p.Phe162Ser) c.482T>C (p.Phe161Ser) c.11T>C (p.Phe4Ser) | |
4 | g.73442298T>G | CA357236388 | AFP | c.485T>G (p.Phe162Cys) c.482T>G (p.Phe161Cys) c.11T>G (p.Phe4Cys) | |
4 | g.73442299C>A | CA357236392 | AFP | c.486C>A (p.Phe162Leu) c.483C>A (p.Phe161Leu) c.12C>A (p.Phe4Leu) | |
4 | g.73442299C>G | CA357236390 | AFP | c.486C>G (p.Phe162Leu) c.483C>G (p.Phe161Leu) c.12C>G (p.Phe4Leu) | |
4 | g.73442299C>T | CA439800123 | AFP | c.486C>T (p.Phe162=) c.483C>T (p.Phe161=) c.12C>T (p.Phe4=) | |
4 | g.73442300A>C | CA357236394 | AFP | c.487A>C (p.Ile163Leu) c.484A>C (p.Ile162Leu) c.13A>C (p.Ile5Leu) | |
4 | g.73442300A>G | CA357236396 | AFP | c.487A>G (p.Ile163Val) c.484A>G (p.Ile162Val) c.13A>G (p.Ile5Val) | |
4 | g.73442300A>T | CA357236398 | AFP | c.487A>T (p.Ile163Phe) c.484A>T (p.Ile162Phe) c.13A>T (p.Ile5Phe) | |
4 | g.73442301T>A | CA357236401 | AFP | c.488T>A (p.Ile163Asn) c.485T>A (p.Ile162Asn) c.14T>A (p.Ile5Asn) | |
4 | g.73442301T>C | CA357236402 | AFP | c.488T>C (p.Ile163Thr) c.485T>C (p.Ile162Thr) c.14T>C (p.Ile5Thr) | |
4 | g.73442301T>G | CA357236404 | AFP | c.488T>G (p.Ile163Ser) c.485T>G (p.Ile162Ser) c.14T>G (p.Ile5Ser) | |
4 | g.73442302T>A | CA439800124 | AFP | c.489T>A (p.Ile163=) c.486T>A (p.Ile162=) c.15T>A (p.Ile5=) | |
4 | g.73442302T>C | CA439800125 | AFP | c.489T>C (p.Ile163=) c.486T>C (p.Ile162=) c.15T>C (p.Ile5=) | |
4 | g.73442302T>G | CA357236406 | AFP | c.489T>G (p.Ile163Met) c.486T>G (p.Ile162Met) c.15T>G (p.Ile5Met) | |
4 | g.73442303T>A | CA357236408 | AFP | c.490T>A (p.Tyr164Asn) c.487T>A (p.Tyr163Asn) c.16T>A (p.Tyr6Asn) | |
4 | g.73442303T>C | CA357236410 | AFP | c.490T>C (p.Tyr164His) c.487T>C (p.Tyr163His) c.16T>C (p.Tyr6His) | |
4 | g.73442303T>G | CA357236412 | AFP | c.490T>G (p.Tyr164Asp) c.487T>G (p.Tyr163Asp) c.16T>G (p.Tyr6Asp) | |
4 | g.73442304A= | CA1468178500 | AFP | c.491A= (p.Tyr164=) c.488A= (p.Tyr163=) c.17A= (p.Tyr6=) | |
4 | g.73442304A>C | CA357236414 | AFP | c.491A>C (p.Tyr164Ser) c.488A>C (p.Tyr163Ser) c.17A>C (p.Tyr6Ser) | |
4 | g.73442304A>G | CA357236416 | AFP | c.491A>G (p.Tyr164Cys) c.488A>G (p.Tyr163Cys) c.17A>G (p.Tyr6Cys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442304A>T | CA357236418 | AFP | c.491A>T (p.Tyr164Phe) c.488A>T (p.Tyr163Phe) c.17A>T (p.Tyr6Phe) | |
4 | g.73442305T>A | CA357236421 | AFP | c.492T>A (p.Tyr164Ter) c.489T>A (p.Tyr163Ter) c.18T>A (p.Tyr6Ter) | gnomAD v4 |
4 | g.73442305T>C | CA439800126 | AFP | c.492T>C (p.Tyr164=) c.489T>C (p.Tyr163=) c.18T>C (p.Tyr6=) | gnomAD v4 |
4 | g.73442305T>G | CA357236423 | AFP | c.492T>G (p.Tyr164Ter) c.489T>G (p.Tyr163Ter) c.18T>G (p.Tyr6Ter) | |
4 | g.73442306G>A | CA357236425 | AFP | c.493G>A (p.Glu165Lys) c.490G>A (p.Glu164Lys) c.19G>A (p.Glu7Lys) | |
4 | g.73442306G>C | CA357236427 | AFP | c.493G>C (p.Glu165Gln) c.490G>C (p.Glu164Gln) c.19G>C (p.Glu7Gln) | gnomAD v4 |
4 | g.73442306G>T | CA357236429 | AFP | c.493G>T (p.Glu165Ter) c.490G>T (p.Glu164Ter) c.19G>T (p.Glu7Ter) | |
4 | g.73442307A>C | CA357236431 | AFP | c.494A>C (p.Glu165Ala) c.491A>C (p.Glu164Ala) c.20A>C (p.Glu7Ala) | |
4 | g.73442307A>G | CA357236433 | AFP | c.494A>G (p.Glu165Gly) c.491A>G (p.Glu164Gly) c.20A>G (p.Glu7Gly) | |
4 | g.73442307A>T | CA357236435 | AFP | c.494A>T (p.Glu165Val) c.491A>T (p.Glu164Val) c.20A>T (p.Glu7Val) | |
4 | g.73442308G>A | CA439800127 | AFP | c.495G>A (p.Glu165=) c.492G>A (p.Glu164=) c.21G>A (p.Glu7=) | gnomAD v4 |
4 | g.73442308G>C | CA357236437 | AFP | c.495G>C (p.Glu165Asp) c.492G>C (p.Glu164Asp) c.21G>C (p.Glu7Asp) | |
4 | g.73442308G>T | CA357236439 | AFP | c.495G>T (p.Glu165Asp) c.492G>T (p.Glu164Asp) c.21G>T (p.Glu7Asp) | |
4 | g.73442309A= | CA1468178506 | AFP | c.496A= (p.Ile166=) c.493A= (p.Ile165=) c.22A= (p.Ile8=) | |
4 | g.73442309A>C | CA357236441 | AFP | c.496A>C (p.Ile166Leu) c.493A>C (p.Ile165Leu) c.22A>C (p.Ile8Leu) | |
4 | g.73442309A>G | CA99671542 | AFP | c.496A>G (p.Ile166Val) c.493A>G (p.Ile165Val) c.22A>G (p.Ile8Val) | dbSNP |
4 | g.73442309A>T | CA357236443 | AFP | c.496A>T (p.Ile166Leu) c.493A>T (p.Ile165Leu) c.22A>T (p.Ile8Leu) | |
4 | g.73442310T>A | CA357236446 | AFP | c.497T>A (p.Ile166Lys) c.494T>A (p.Ile165Lys) c.23T>A (p.Ile8Lys) | |
4 | g.73442310T>C | CA357236448 | AFP | c.497T>C (p.Ile166Thr) c.494T>C (p.Ile165Thr) c.23T>C (p.Ile8Thr) | dbSNP gnomAD v4 |
4 | g.73442310T>G | CA357236451 | AFP | c.497T>G (p.Ile166Arg) c.494T>G (p.Ile165Arg) c.23T>G (p.Ile8Arg) | |
4 | g.73442311A>C | CA439800128 | AFP | c.498A>C (p.Ile166=) c.495A>C (p.Ile165=) c.24A>C (p.Ile8=) | |
4 | g.73442311A>G | CA357236452 | AFP | c.498A>G (p.Ile166Met) c.495A>G (p.Ile165Met) c.24A>G (p.Ile8Met) | |
4 | g.73442311A>T | CA439800129 | AFP | c.498A>T (p.Ile166=) c.495A>T (p.Ile165=) c.24A>T (p.Ile8=) | |
4 | g.73442312G>A | CA357236455 | AFP | c.499G>A (p.Ala167Thr) c.496G>A (p.Ala166Thr) c.25G>A (p.Ala9Thr) | |
4 | g.73442312G>C | CA357236459 | AFP | c.499G>C (p.Ala167Pro) c.496G>C (p.Ala166Pro) c.25G>C (p.Ala9Pro) | |
4 | g.73442312G>T | CA357236457 | AFP | c.499G>T (p.Ala167Ser) c.496G>T (p.Ala166Ser) c.25G>T (p.Ala9Ser) | |
4 | g.73442313C>A | CA357236461 | AFP | c.500C>A (p.Ala167Glu) c.497C>A (p.Ala166Glu) c.26C>A (p.Ala9Glu) | |
4 | g.73442313C= | CA1468178509 | AFP | c.500C= (p.Ala167=) c.497C= (p.Ala166=) c.26C= (p.Ala9=) | |
4 | g.73442313C>G | CA357236463 | AFP | c.500C>G (p.Ala167Gly) c.497C>G (p.Ala166Gly) c.26C>G (p.Ala9Gly) | |
4 | g.73442313C>T | CA99671551 | AFP | c.500C>T (p.Ala167Val) c.497C>T (p.Ala166Val) c.26C>T (p.Ala9Val) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.73442314A>C | CA439800130 | AFP | c.501A>C (p.Ala167=) c.498A>C (p.Ala166=) c.27A>C (p.Ala9=) | |
4 | g.73442314A>G | CA439800131 | AFP | c.501A>G (p.Ala167=) c.498A>G (p.Ala166=) c.27A>G (p.Ala9=) | |
4 | g.73442314A>T | CA439800132 | AFP | c.501A>T (p.Ala167=) c.498A>T (p.Ala166=) c.27A>T (p.Ala9=) | |
4 | g.73442315A>C | CA439800133 | AFP | c.502A>C (p.Arg168=) c.499A>C (p.Arg167=) c.28A>C (p.Arg10=) | |
4 | g.73442315A>G | CA357236466 | AFP | c.502A>G (p.Arg168Gly) c.499A>G (p.Arg167Gly) c.28A>G (p.Arg10Gly) | |
4 | g.73442315A>T | CA357236468 | AFP | c.502A>T (p.Arg168Ter) c.499A>T (p.Arg167Ter) c.28A>T (p.Arg10Ter) | |
4 | g.73442316G>A | CA357236470 | AFP | c.503G>A (p.Arg168Lys) c.500G>A (p.Arg167Lys) c.29G>A (p.Arg10Lys) | |
4 | g.73442316G>C | CA357236472 | AFP | c.503G>C (p.Arg168Thr) c.500G>C (p.Arg167Thr) c.29G>C (p.Arg10Thr) | |
4 | g.73442316G>T | CA357236474 | AFP | c.503G>T (p.Arg168Ile) c.500G>T (p.Arg167Ile) c.29G>T (p.Arg10Ile) | |
4 | g.73442317A>C | CA357236476 | AFP | c.504A>C (p.Arg168Ser) c.501A>C (p.Arg167Ser) c.30A>C (p.Arg10Ser) | |
4 | g.73442317A>G | CA439800134 | AFP | c.504A>G (p.Arg168=) c.501A>G (p.Arg167=) c.30A>G (p.Arg10=) | gnomAD v4 |
4 | g.73442317A>T | CA357236478 | AFP | c.504A>T (p.Arg168Ser) c.501A>T (p.Arg167Ser) c.30A>T (p.Arg10Ser) | |
4 | g.73442318A>C | CA439800135 | AFP | c.505A>C (p.Arg169=) c.502A>C (p.Arg168=) c.31A>C (p.Arg11=) | |
4 | g.73442318A>G | CA357236481 | AFP | c.505A>G (p.Arg169Gly) c.502A>G (p.Arg168Gly) c.31A>G (p.Arg11Gly) | |
4 | g.73442318A>T | CA357236482 | AFP | c.505A>T (p.Arg169Trp) c.502A>T (p.Arg168Trp) c.31A>T (p.Arg11Trp) | |
4 | g.73442319G>A | CA2959937 | AFP | c.506G>A (p.Arg169Lys) c.503G>A (p.Arg168Lys) c.32G>A (p.Arg11Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442319G>C | CA357236486 | AFP | c.506G>C (p.Arg169Thr) c.503G>C (p.Arg168Thr) c.32G>C (p.Arg11Thr) | |
4 | g.73442319G= | CA1468178514 | AFP | c.506G= (p.Arg169=) c.503G= (p.Arg168=) c.32G= (p.Arg11=) | |
4 | g.73442319G>T | CA357236484 | AFP | c.506G>T (p.Arg169Met) c.503G>T (p.Arg168Met) c.32G>T (p.Arg11Met) | |
4 | g.73442320G>A | CA439800136 | AFP | c.507G>A (p.Arg169=) c.504G>A (p.Arg168=) c.33G>A (p.Arg11=) | gnomAD v4 |
4 | g.73442320G>C | CA357236488 | AFP | c.507G>C (p.Arg169Ser) c.504G>C (p.Arg168Ser) c.33G>C (p.Arg11Ser) | |
4 | g.73442320G= | CA1468178516 | AFP | c.507G= (p.Arg169=) c.504G= (p.Arg168=) c.33G= (p.Arg11=) | |
4 | g.73442320G>T | CA357236490 | AFP | c.507G>T (p.Arg169Ser) c.504G>T (p.Arg168Ser) c.33G>T (p.Arg11Ser) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.73442321C>A | CA357236492 | AFP | c.508C>A (p.His170Asn) c.505C>A (p.His169Asn) c.34C>A (p.His12Asn) | |
4 | g.73442321C>G | CA357236494 | AFP | c.508C>G (p.His170Asp) c.505C>G (p.His169Asp) c.34C>G (p.His12Asp) | |
4 | g.73442321C>T | CA357236496 | AFP | c.508C>T (p.His170Tyr) c.505C>T (p.His169Tyr) c.34C>T (p.His12Tyr) | |
4 | g.73442322A= | CA1468178520 | AFP | c.509A= (p.His170=) c.506A= (p.His169=) c.35A= (p.His12=) | |
4 | g.73442322A>C | CA357236498 | AFP | c.509A>C (p.His170Pro) c.506A>C (p.His169Pro) c.35A>C (p.His12Pro) | |
4 | g.73442322A>G | CA2959938 | AFP | c.509A>G (p.His170Arg) c.506A>G (p.His169Arg) c.35A>G (p.His12Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442322A>T | CA357236501 | AFP | c.509A>T (p.His170Leu) c.506A>T (p.His169Leu) c.35A>T (p.His12Leu) | |
4 | g.73442323T>A | CA357236503 | AFP | c.510T>A (p.His170Gln) c.507T>A (p.His169Gln) c.36T>A (p.His12Gln) | gnomAD v4 |
4 | g.73442323T>C | CA439800137 | AFP | c.510T>C (p.His170=) c.507T>C (p.His169=) c.36T>C (p.His12=) | dbSNP gnomAD v4 |
4 | g.73442323T>G | CA357236505 | AFP | c.510T>G (p.His170Gln) c.507T>G (p.His169Gln) c.36T>G (p.His12Gln) | |
4 | g.73442324C>A | CA357236507 | AFP | c.511C>A (p.Pro171Thr) c.508C>A (p.Pro170Thr) c.37C>A (p.Pro13Thr) | gnomAD v4 |
4 | g.73442324C= | CA1468178522 | AFP | c.511C= (p.Pro171=) c.508C= (p.Pro170=) c.37C= (p.Pro13=) | |
4 | g.73442324C>G | CA357236509 | AFP | c.511C>G (p.Pro171Ala) c.508C>G (p.Pro170Ala) c.37C>G (p.Pro13Ala) | |
4 | g.73442324C>T | CA357236511 | AFP | c.511C>T (p.Pro171Ser) c.508C>T (p.Pro170Ser) c.37C>T (p.Pro13Ser) | dbSNP gnomAD v4 |
4 | g.73442325C>A | CA357236513 | AFP | c.512C>A (p.Pro171His) c.509C>A (p.Pro170His) c.38C>A (p.Pro13His) | gnomAD v4 |
4 | g.73442325C= | CA1468178524 | AFP | c.512C= (p.Pro171=) c.509C= (p.Pro170=) c.38C= (p.Pro13=) | |
4 | g.73442325C>G | CA2959939 | AFP | c.512C>G (p.Pro171Arg) c.509C>G (p.Pro170Arg) c.38C>G (p.Pro13Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442325C>T | CA357236514 | AFP | c.512C>T (p.Pro171Leu) c.509C>T (p.Pro170Leu) c.38C>T (p.Pro13Leu) | |
4 | g.73442326C>A | CA439800138 | AFP | c.513C>A (p.Pro171=) c.510C>A (p.Pro170=) c.39C>A (p.Pro13=) | |
4 | g.73442326C>G | CA439800140 | AFP | c.513C>G (p.Pro171=) c.510C>G (p.Pro170=) c.39C>G (p.Pro13=) | |
4 | g.73442326C>T | CA439800139 | AFP | c.513C>T (p.Pro171=) c.510C>T (p.Pro170=) c.39C>T (p.Pro13=) | |
4 | g.73442327T>A | CA357236517 | AFP | c.514T>A (p.Phe172Ile) c.511T>A (p.Phe171Ile) c.40T>A (p.Phe14Ile) | |
4 | g.73442327T>C | CA357236518 | AFP | c.514T>C (p.Phe172Leu) c.511T>C (p.Phe171Leu) c.40T>C (p.Phe14Leu) | |
4 | g.73442327T>G | CA357236519 | AFP | c.514T>G (p.Phe172Val) c.511T>G (p.Phe171Val) c.40T>G (p.Phe14Val) | |
4 | g.73442328T>A | CA357236522 | AFP | c.515T>A (p.Phe172Tyr) c.512T>A (p.Phe171Tyr) c.41T>A (p.Phe14Tyr) | |
4 | g.73442328T>C | CA357236524 | AFP | c.515T>C (p.Phe172Ser) c.512T>C (p.Phe171Ser) c.41T>C (p.Phe14Ser) | |
4 | g.73442328T>G | CA357236525 | AFP | c.515T>G (p.Phe172Cys) c.512T>G (p.Phe171Cys) c.41T>G (p.Phe14Cys) | |
4 | g.73442329C>A | CA357236527 | AFP | c.516C>A (p.Phe172Leu) c.513C>A (p.Phe171Leu) c.42C>A (p.Phe14Leu) | |
4 | g.73442329C= | CA1468178527 | AFP | c.516C= (p.Phe172=) c.513C= (p.Phe171=) c.42C= (p.Phe14=) | |
4 | g.73442329C>G | CA357236528 | AFP | c.516C>G (p.Phe172Leu) c.513C>G (p.Phe171Leu) c.42C>G (p.Phe14Leu) | |
4 | g.73442329C>T | CA439800141 | AFP | c.516C>T (p.Phe172=) c.513C>T (p.Phe171=) c.42C>T (p.Phe14=) | dbSNP gnomAD v4 |
4 | g.73442330C>A | CA357236531 | AFP | c.517C>A (p.Leu173Met) c.514C>A (p.Leu172Met) c.43C>A (p.Leu15Met) | |
4 | g.73442330C= | CA1468178530 | AFP | c.517C= (p.Leu173=) c.514C= (p.Leu172=) c.43C= (p.Leu15=) | |
4 | g.73442330C>G | CA357236533 | AFP | c.517C>G (p.Leu173Val) c.514C>G (p.Leu172Val) c.43C>G (p.Leu15Val) | |
4 | g.73442330C>T | CA439800142 | AFP | c.517C>T (p.Leu173=) c.514C>T (p.Leu172=) c.43C>T (p.Leu15=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442331T>A | CA357236540 | AFP | c.518T>A (p.Leu173Gln) c.515T>A (p.Leu172Gln) c.44T>A (p.Leu15Gln) | |
4 | g.73442331T>C | CA357236538 | AFP | c.518T>C (p.Leu173Pro) c.515T>C (p.Leu172Pro) c.44T>C (p.Leu15Pro) | |
4 | g.73442331T>G | CA357236536 | AFP | c.518T>G (p.Leu173Arg) c.515T>G (p.Leu172Arg) c.44T>G (p.Leu15Arg) | |
4 | g.73442332G>A | CA2959940 | AFP | c.519G>A (p.Leu173=) c.516G>A (p.Leu172=) c.45G>A (p.Leu15=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.73442332G>C | CA2959941 | AFP | c.519G>C (p.Leu173=) c.516G>C (p.Leu172=) c.45G>C (p.Leu15=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.73442332G= | CA1468178537 | AFP | c.519G= (p.Leu173=) c.516G= (p.Leu172=) c.45G= (p.Leu15=) | |
4 | g.73442332G>T | CA439800143 | AFP | c.519G>T (p.Leu173=) c.516G>T (p.Leu172=) c.45G>T (p.Leu15=) | |
4 | g.73442333T>A | CA357236544 | AFP | c.520T>A (p.Tyr174Asn) c.517T>A (p.Tyr173Asn) c.46T>A (p.Tyr16Asn) | dbSNP |
4 | g.73442333T>C | CA357236548 | AFP | c.520T>C (p.Tyr174His) c.517T>C (p.Tyr173His) c.46T>C (p.Tyr16His) | |
4 | g.73442333T>G | CA357236546 | AFP | c.520T>G (p.Tyr174Asp) c.517T>G (p.Tyr173Asp) c.46T>G (p.Tyr16Asp) | |
4 | g.73442333T= | CA1468178542 | AFP | c.520T= (p.Tyr174=) c.517T= (p.Tyr173=) c.46T= (p.Tyr16=) | |
4 | g.73442334A>C | CA357236550 | AFP | c.521A>C (p.Tyr174Ser) c.518A>C (p.Tyr173Ser) c.47A>C (p.Tyr16Ser) | |
4 | g.73442334A>G | CA357236554 | AFP | c.521A>G (p.Tyr174Cys) c.518A>G (p.Tyr173Cys) c.47A>G (p.Tyr16Cys) | gnomAD v4 |
4 | g.73442334A>T | CA357236552 | AFP | c.521A>T (p.Tyr174Phe) c.518A>T (p.Tyr173Phe) c.47A>T (p.Tyr16Phe) | |
4 | g.73442335T>A | CA357236556 | AFP | c.522T>A (p.Tyr174Ter) c.519T>A (p.Tyr173Ter) c.48T>A (p.Tyr16Ter) | |
4 | g.73442335T>C | CA2959942 | AFP | c.522T>C (p.Tyr174=) c.519T>C (p.Tyr173=) c.48T>C (p.Tyr16=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.73442335T>G | CA357236558 | AFP | c.522T>G (p.Tyr174Ter) c.519T>G (p.Tyr173Ter) c.48T>G (p.Tyr16Ter) | |
4 | g.73442335T= | CA1468178543 | AFP | c.522T= (p.Tyr174=) c.519T= (p.Tyr173=) c.48T= (p.Tyr16=) | |
4 | g.73442336G>A | CA357236560 | AFP | c.523G>A (p.Ala175Thr) c.520G>A (p.Ala174Thr) c.49G>A (p.Ala17Thr) | |
4 | g.73442336G>C | CA357236564 | AFP | c.523G>C (p.Ala175Pro) c.520G>C (p.Ala174Pro) c.49G>C (p.Ala17Pro) | |
4 | g.73442336G= | CA1468178546 | AFP | c.523G= (p.Ala175=) c.520G= (p.Ala174=) c.49G= (p.Ala17=) | |
4 | g.73442336G>T | CA357236562 | AFP | c.523G>T (p.Ala175Ser) c.520G>T (p.Ala174Ser) c.49G>T (p.Ala17Ser) | dbSNP |
4 | g.73442337C>A | CA357236566 | AFP | c.524C>A (p.Ala175Glu) c.521C>A (p.Ala174Glu) c.50C>A (p.Ala17Glu) | |
4 | g.73442337C>G | CA357236568 | AFP | c.524C>G (p.Ala175Gly) c.521C>G (p.Ala174Gly) c.50C>G (p.Ala17Gly) | |
4 | g.73442337C>T | CA357236570 | AFP | c.524C>T (p.Ala175Val) c.521C>T (p.Ala174Val) c.50C>T (p.Ala17Val) | gnomAD v4 |
4 | g.73442338A= | CA1468178550 | AFP | c.525A= (p.Ala175=) c.522A= (p.Ala174=) c.51A= (p.Ala17=) | |
4 | g.73442338A>C | CA2959943 | AFP | c.525A>C (p.Ala175=) c.522A>C (p.Ala174=) c.51A>C (p.Ala17=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442338A>G | CA439800145 | AFP | c.525A>G (p.Ala175=) c.522A>G (p.Ala174=) c.51A>G (p.Ala17=) | |
4 | g.73442338A>T | CA439800146 | AFP | c.525A>T (p.Ala175=) c.522A>T (p.Ala174=) c.51A>T (p.Ala17=) | |
4 | g.73442339C>A | CA2959944 | AFP | c.526C>A (p.Pro176Thr) c.523C>A (p.Pro175Thr) c.52C>A (p.Pro18Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442339C= | CA1468178554 | AFP | c.526C= (p.Pro176=) c.523C= (p.Pro175=) c.52C= (p.Pro18=) | |
4 | g.73442339C>G | CA357236575 | AFP | c.526C>G (p.Pro176Ala) c.523C>G (p.Pro175Ala) c.52C>G (p.Pro18Ala) | |
4 | g.73442339C>T | CA357236577 | AFP | c.526C>T (p.Pro176Ser) c.523C>T (p.Pro175Ser) c.52C>T (p.Pro18Ser) | |
4 | g.73442340C>A | CA357236579 | AFP | c.527C>A (p.Pro176His) c.524C>A (p.Pro175His) c.53C>A (p.Pro18His) | |
4 | g.73442340C>G | CA357236584 | AFP | c.527C>G (p.Pro176Arg) c.524C>G (p.Pro175Arg) c.53C>G (p.Pro18Arg) | |
4 | g.73442340C>T | CA357236585 | AFP | c.527C>T (p.Pro176Leu) c.524C>T (p.Pro175Leu) c.53C>T (p.Pro18Leu) | |
4 | g.73442341T>A | CA439800151 | AFP | c.528T>A (p.Pro176=) c.525T>A (p.Pro175=) c.54T>A (p.Pro18=) | |
4 | g.73442341T>C | CA439800150 | AFP | c.528T>C (p.Pro176=) c.525T>C (p.Pro175=) c.54T>C (p.Pro18=) | |
4 | g.73442341T>G | CA439800148 | AFP | c.528T>G (p.Pro176=) c.525T>G (p.Pro175=) c.54T>G (p.Pro18=) | |
4 | g.73442342A= | CA1468178556 | AFP | c.529A= (p.Thr177=) c.526A= (p.Thr176=) c.55A= (p.Thr19=) | |
4 | g.73442342A>C | CA357236588 | AFP | c.529A>C (p.Thr177Pro) c.526A>C (p.Thr176Pro) c.55A>C (p.Thr19Pro) | |
4 | g.73442342A>G | CA357236590 | AFP | c.529A>G (p.Thr177Ala) c.526A>G (p.Thr176Ala) c.55A>G (p.Thr19Ala) | dbSNP gnomAD v2 |
4 | g.73442342A>T | CA357236591 | AFP | c.529A>T (p.Thr177Ser) c.526A>T (p.Thr176Ser) c.55A>T (p.Thr19Ser) | |
4 | g.73442343C>A | CA2959945 | AFP | c.530C>A (p.Thr177Lys) c.527C>A (p.Thr176Lys) c.56C>A (p.Thr19Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.73442343C= | CA1468178560 | AFP | c.530C= (p.Thr177=) c.527C= (p.Thr176=) c.56C= (p.Thr19=) | |
4 | g.73442343C>G | CA99671577 | AFP | c.530C>G (p.Thr177Arg) c.527C>G (p.Thr176Arg) c.56C>G (p.Thr19Arg) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.73442343C>T | CA357236594 | AFP | c.530C>T (p.Thr177Ile) c.527C>T (p.Thr176Ile) c.56C>T (p.Thr19Ile) | |
4 | g.73442344A>C | CA439800156 | AFP | c.531A>C (p.Thr177=) c.528A>C (p.Thr176=) c.57A>C (p.Thr19=) | |
4 | g.73442344A>G | CA439800157 | AFP | c.531A>G (p.Thr177=) c.528A>G (p.Thr176=) c.57A>G (p.Thr19=) | |
4 | g.73442344A>T | CA439800158 | AFP | c.531A>T (p.Thr177=) c.528A>T (p.Thr176=) c.57A>T (p.Thr19=) | |
4 | g.73442345A= | CA1468178565 | AFP | c.532A= (p.Ile178=) c.529A= (p.Ile177=) c.58A= (p.Ile20=) | |
4 | g.73442345A>C | CA357236595 | AFP | c.532A>C (p.Ile178Leu) c.529A>C (p.Ile177Leu) c.58A>C (p.Ile20Leu) | |
4 | g.73442345A>G | CA357236596 | AFP | c.532A>G (p.Ile178Val) c.529A>G (p.Ile177Val) c.58A>G (p.Ile20Val) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.73442345A>T | CA357236597 | AFP | c.532A>T (p.Ile178Phe) c.529A>T (p.Ile177Phe) c.58A>T (p.Ile20Phe) | |
4 | g.73442346T>A | CA357236599 | AFP | c.533T>A (p.Ile178Asn) c.530T>A (p.Ile177Asn) c.59T>A (p.Ile20Asn) | |
4 | g.73442346T>C | CA357236601 | AFP | c.533T>C (p.Ile178Thr) c.530T>C (p.Ile177Thr) c.59T>C (p.Ile20Thr) | |
4 | g.73442346T>G | CA357236603 | AFP | c.533T>G (p.Ile178Ser) c.530T>G (p.Ile177Ser) c.59T>G (p.Ile20Ser) | |
4 | g.73442351_73442353del | CA2670968531 | AFP | c.538_540del (p.Leu180del) c.535_537del (p.Leu179del) c.64_66del (p.Leu22del) | gnomAD v4 |
4 | g.73442347T>A | CA439800163 | AFP | c.534T>A (p.Ile178=) c.531T>A (p.Ile177=) c.60T>A (p.Ile20=) | |
4 | g.73442347T>C | CA439800162 | AFP | c.534T>C (p.Ile178=) c.531T>C (p.Ile177=) c.60T>C (p.Ile20=) | |
4 | g.73442347T>G | CA357236604 | AFP | c.534T>G (p.Ile178Met) c.531T>G (p.Ile177Met) c.60T>G (p.Ile20Met) | |
4 | g.73442348C>A | CA357236606 | AFP | c.535C>A (p.Leu179Ile) c.532C>A (p.Leu178Ile) c.61C>A (p.Leu21Ile) | COSMIC |
4 | g.73442348C>G | CA357236612 | AFP | c.535C>G (p.Leu179Val) c.532C>G (p.Leu178Val) c.61C>G (p.Leu21Val) | |
4 | g.73442348C>T | CA357236614 | AFP | c.535C>T (p.Leu179Phe) c.532C>T (p.Leu178Phe) c.61C>T (p.Leu21Phe) | |
4 | g.73442348_73442352delinsCTTCT | CA1468178569 | AFP | c.535_539delinsCTTCT (p.Leu179=) c.532_536delinsCTTCT (p.Leu178=) c.61_65delinsCTTCT (p.Leu21=) | |
4 | g.73442349T>A | CA357236619 | AFP | c.536T>A (p.Leu179His) c.533T>A (p.Leu178His) c.62T>A (p.Leu21His) | |
4 | g.73442349T>C | CA357236617 | AFP | c.536T>C (p.Leu179Pro) c.533T>C (p.Leu178Pro) c.62T>C (p.Leu21Pro) | |
4 | g.73442349T>G | CA357236615 | AFP | c.536T>G (p.Leu179Arg) c.533T>G (p.Leu178Arg) c.62T>G (p.Leu21Arg) | |
4 | g.73442350dup | CA2512019574 | AFP | c.537dup (p.Leu180SerfsTer7) c.534dup (p.Leu179SerfsTer7) c.63dup (p.Leu22SerfsTer7) | |
4 | g.73442351_73442354del | CA798266796 | AFP | c.538_541del (p.Leu180GlyfsTer8) c.535_538del (p.Leu179GlyfsTer8) c.64_67del (p.Leu22GlyfsTer8) | dbSNP |
4 | g.73442350T>A | CA439800167 | AFP | c.537T>A (p.Leu179=) c.534T>A (p.Leu178=) c.63T>A (p.Leu21=) | |
4 | g.73442350T>C | CA439800168 | AFP | c.537T>C (p.Leu179=) c.534T>C (p.Leu178=) c.63T>C (p.Leu21=) | |
4 | g.73442350T>G | CA439800169 | AFP | c.537T>G (p.Leu179=) c.534T>G (p.Leu178=) c.63T>G (p.Leu21=) | |
4 | g.73442351C>A | CA357236623 | AFP | c.538C>A (p.Leu180Ile) c.535C>A (p.Leu179Ile) c.64C>A (p.Leu22Ile) | COSMIC |
4 | g.73442351C>G | CA357236620 | AFP | c.538C>G (p.Leu180Val) c.535C>G (p.Leu179Val) c.64C>G (p.Leu22Val) | |
4 | g.73442351C>T | CA357236621 | AFP | c.538C>T (p.Leu180Phe) c.535C>T (p.Leu179Phe) c.64C>T (p.Leu22Phe) | |
4 | g.73442352T>A | CA357236626 | AFP | c.539T>A (p.Leu180His) c.536T>A (p.Leu179His) c.65T>A (p.Leu22His) | |
4 | g.73442352T>C | CA357236628 | AFP | c.539T>C (p.Leu180Pro) c.536T>C (p.Leu179Pro) c.65T>C (p.Leu22Pro) | |
4 | g.73442352T>G | CA357236630 | AFP | c.539T>G (p.Leu180Arg) c.536T>G (p.Leu179Arg) c.65T>G (p.Leu22Arg) | |
4 | g.73442353T>A | CA439800173 | AFP | c.540T>A (p.Leu180=) c.537T>A (p.Leu179=) c.66T>A (p.Leu22=) | |
4 | g.73442353T>C | CA439800171 | AFP | c.540T>C (p.Leu180=) c.537T>C (p.Leu179=) c.66T>C (p.Leu22=) | dbSNP |
4 | g.73442353T>G | CA439800172 | AFP | c.540T>G (p.Leu180=) c.537T>G (p.Leu179=) c.66T>G (p.Leu22=) | |
4 | g.73442353T= | CA1468178575 | AFP | c.540T= (p.Leu180=) c.537T= (p.Leu179=) c.66T= (p.Leu22=) | |
4 | g.73442354T>A | CA357236636 | AFP | c.541T>A (p.Trp181Arg) c.538T>A (p.Trp180Arg) c.67T>A (p.Trp23Arg) | |
4 | g.73442354T>C | CA357236634 | AFP | c.541T>C (p.Trp181Arg) c.538T>C (p.Trp180Arg) c.67T>C (p.Trp23Arg) | |
4 | g.73442354T>G | CA357236632 | AFP | c.541T>G (p.Trp181Gly) c.538T>G (p.Trp180Gly) c.67T>G (p.Trp23Gly) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.73442354T= | CA1468178579 | AFP | c.541T= (p.Trp181=) c.538T= (p.Trp180=) c.67T= (p.Trp23=) | |
4 | g.73442355G>A | CA357236637 | AFP | c.542G>A (p.Trp181Ter) c.539G>A (p.Trp180Ter) c.68G>A (p.Trp23Ter) | |
4 | g.73442355G>C | CA357236638 | AFP | c.542G>C (p.Trp181Ser) c.539G>C (p.Trp180Ser) c.68G>C (p.Trp23Ser) | |
4 | g.73442355G= | CA1468178581 | AFP | c.542G= (p.Trp181=) c.539G= (p.Trp180=) c.68G= (p.Trp23=) | |
4 | g.73442355G>T | CA99671581 | AFP | c.542G>T (p.Trp181Leu) c.539G>T (p.Trp180Leu) c.68G>T (p.Trp23Leu) | dbSNP |
4 | g.73442357del | CA2531045514 | AFP | c.544del (p.Ala182LeufsTer7) c.541del (p.Ala181LeufsTer7) c.70del (p.Ala24LeufsTer7) |