Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.41348276T>C | CA2840843128 | TGFB1 | c.516+19A>G (n.516+19A>G) n.47+19A>G | |
19 | g.41348276T>G | CA882319758 | TGFB1 | c.516+19A>C (n.516+19A>C) n.47+19A>C | ClinVar dbSNP |
19 | g.41348276T= | CA2336423931 | TGFB1 | c.516+19A= (n.516+19A=) n.47+19A= | |
19 | g.41348278C= | CA2336423932 | TGFB1 | c.516+17G= (n.516+17G=) n.47+17G= | |
19 | g.41348278C>T | CA633167507 | TGFB1 | c.516+17G>A (n.516+17G>A) n.47+17G>A | dbSNP gnomAD v2 |
19 | g.41348280G>T | CA2840843130 | TGFB1 | c.516+15C>A (n.516+15C>A) n.47+15C>A | |
19 | g.41348281del | CA2840843129 | TGFB1 | c.516+15del (n.516+15del) n.47+15del | |
19 | g.41348281G>A | CA2573156383 | TGFB1 | c.516+14C>T (n.516+14C>T) n.47+14C>T | ClinVar dbSNP gnomAD v4 |
19 | g.41348281G>C | CA2838808466 | TGFB1 | c.516+14C>G (n.516+14C>G) n.47+14C>G | |
19 | g.41348282C>A | CA2840843131 | TGFB1 | c.516+13G>T (n.516+13G>T) n.47+13G>T | |
19 | g.41348283T>C | CA2585296890 | TGFB1 | c.516+12A>G (n.516+12A>G) n.47+12A>G | gnomAD v4 |
19 | g.41348284C>G | CA2585296891 | TGFB1 | c.516+11G>C (n.516+11G>C) n.47+11G>C | gnomAD v4 |
19 | g.41348284C>T | CA2585296892 | TGFB1 | c.516+11G>A (n.516+11G>A) n.47+11G>A | gnomAD v4 |
19 | g.41348284_41348285dup | CA2509689226 | TGFB1 | c.516+10_516+11dup (n.516+10_516+11dup) n.47+10_47+11dup | |
19 | g.41348285A= | CA2336423933 | TGFB1 | c.516+10T= (n.516+10T=) n.47+10T= | |
19 | g.41348285A>C | CA308515253 | TGFB1 | c.516+10T>G (n.516+10T>G) n.47+10T>G | dbSNP |
19 | g.41348285A>G | CA633167508 | TGFB1 | c.516+10T>C (n.516+10T>C) n.47+10T>C | dbSNP gnomAD v2 gnomAD v4 |
19 | g.41348285A>T | CA2840843132 | TGFB1 | c.516+10T>A (n.516+10T>A) n.47+10T>A | |
19 | g.41348286T>A | CA2838324489 | TGFB1 | c.516+9A>T (n.516+9A>T) n.47+9A>T | |
19 | g.41348286T>C | CA633167509 | TGFB1 | c.516+9A>G (n.516+9A>G) n.47+9A>G | dbSNP gnomAD v2 gnomAD v4 |
19 | g.41348286T= | CA2336423934 | TGFB1 | c.516+9A= (n.516+9A=) n.47+9A= | |
19 | g.41348287G>A | CA645607129 | TGFB1 | c.516+8C>T (n.516+8C>T) n.47+8C>T | COSMIC |
19 | g.41348289C>A | CA9460079 | TGFB1 | c.516+6G>T (n.516+6G>T) n.47+6G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348289C= | CA2336423935 | TGFB1 | c.516+6G= (n.516+6G=) n.47+6G= | |
19 | g.41348290C= | CA2336423936 | TGFB1 | c.516+5G= (n.516+5G=) n.47+5G= | |
19 | g.41348290C>T | CA882319766 | TGFB1 | c.516+5G>A (n.516+5G>A) n.47+5G>A | dbSNP gnomAD v4 |
19 | g.41348292C>A | CA2840843133 | TGFB1 | c.516+3G>T (n.516+3G>T) n.47+3G>T | |
19 | g.41348292C= | CA2336423937 | TGFB1 | c.516+3G= (n.516+3G=) n.47+3G= | |
19 | g.41348292C>T | CA308515272 | TGFB1 | c.516+3G>A (n.516+3G>A) n.47+3G>A | dbSNP gnomAD v4 |
19 | g.41348293A>C | CA406003420 | TGFB1 | c.516+2T>G (n.516+2T>G) n.47+2T>G | |
19 | g.41348293A>G | CA406003417 | TGFB1 | c.516+2T>C (n.516+2T>C) n.47+2T>C | |
19 | g.41348293A>T | CA406003419 | TGFB1 | c.516+2T>A (n.516+2T>A) n.47+2T>A | |
19 | g.41348294C>A | CA406003421 | TGFB1 | c.516+1G>T (n.516+1G>T) n.47+1G>T | |
19 | g.41348294C= | CA2336423938 | TGFB1 | c.516+1G= (n.516+1G=) n.47+1G= | |
19 | g.41348294C>G | CA406003423 | TGFB1 | c.516+1G>C (n.516+1G>C) n.47+1G>C | |
19 | g.41348294C>T | CA9460080 | TGFB1 | c.516+1G>A (n.516+1G>A) n.47+1G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348295C>A | CA406003426 | TGFB1 | c.516G>T (p.Gln172His) n.47G>T | |
19 | g.41348295C>G | CA406003427 | TGFB1 | c.516G>C (p.Gln172His) n.47G>C | |
19 | g.41348295C>T | CA507555425 | TGFB1 | c.516G>A (p.Gln172=) n.47G>A | |
19 | g.41348296T>A | CA406003428 | TGFB1 | c.515A>T (p.Gln172Leu) n.46A>T | |
19 | g.41348296T>C | CA406003429 | TGFB1 | c.515A>G (p.Gln172Arg) n.46A>G | |
19 | g.41348296T>G | CA406003431 | TGFB1 | c.515A>C (p.Gln172Pro) n.46A>C | |
19 | g.41348297G>A | CA406003433 | TGFB1 | c.514C>T (p.Gln172Ter) n.45C>T | |
19 | g.41348297G>C | CA406003434 | TGFB1 | c.514C>G (p.Gln172Glu) n.45C>G | |
19 | g.41348297G>T | CA406003436 | TGFB1 | c.514C>A (p.Gln172Lys) n.45C>A | |
19 | g.41348297_41348309delinsGGTACAGCTCCAC | CA2336423939 | TGFB1 | c.502_514delinsGTGGAGCTGTACC (p.Val168=) n.33_45delinsGTGGAGCTGTACC | |
19 | g.41348298G>A | CA9460082 | TGFB1 | c.513C>T (p.Tyr171=) n.44C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.41348298G>C | CA406003443 | TGFB1 | c.513C>G (p.Tyr171Ter) n.44C>G | |
19 | g.41348298G= | CA2336423940 | TGFB1 | c.513C= (p.Tyr171=) n.44C= | |
19 | g.41348298G>T | CA406003442 | TGFB1 | c.513C>A (p.Tyr171Ter) n.44C>A | |
19 | g.41348300_41348311del | CA9460081 | TGFB1 | c.502_513del (p.Val168_Tyr171del) n.33_44del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.41348299T>A | CA406003445 | TGFB1 | c.512A>T (p.Tyr171Phe) n.43A>T | |
19 | g.41348299T>C | CA406003447 | TGFB1 | c.512A>G (p.Tyr171Cys) n.43A>G | ClinVar dbSNP |
19 | g.41348299T>G | CA406003449 | TGFB1 | c.512A>C (p.Tyr171Ser) n.43A>C | |
19 | g.41348299T= | CA2336423941 | TGFB1 | c.512A= (p.Tyr171=) n.43A= | |
19 | g.41348300A= | CA2336423942 | TGFB1 | c.511T= (p.Tyr171=) n.42T= | |
19 | g.41348300A>C | CA406003453 | TGFB1 | c.511T>G (p.Tyr171Asp) n.42T>G | |
19 | g.41348300A>G | CA406003451 | TGFB1 | c.511T>C (p.Tyr171His) n.42T>C | dbSNP gnomAD v4 |
19 | g.41348300A>T | CA406003452 | TGFB1 | c.511T>A (p.Tyr171Asn) n.42T>A | |
19 | g.41348301C>A | CA507555428 | TGFB1 | c.510G>T (p.Leu170=) n.41G>T | |
19 | g.41348301C= | CA2336423943 | TGFB1 | c.510G= (p.Leu170=) n.41G= | |
19 | g.41348301C>G | CA507555429 | TGFB1 | c.510G>C (p.Leu170=) n.41G>C | ClinVar dbSNP gnomAD v4 |
19 | g.41348301C>T | CA308515296 | TGFB1 | c.510G>A (p.Leu170=) n.41G>A | dbSNP |
19 | g.41348302A>C | CA406003456 | TGFB1 | c.509T>G (p.Leu170Arg) n.40T>G | |
19 | g.41348302A>G | CA406003458 | TGFB1 | c.509T>C (p.Leu170Pro) n.40T>C | |
19 | g.41348302A>T | CA406003459 | TGFB1 | c.509T>A (p.Leu170Gln) n.40T>A | |
19 | g.41348303G>A | CA507555432 | TGFB1 | c.508C>T (p.Leu170=) n.39C>T | |
19 | g.41348303G>C | CA406003461 | TGFB1 | c.508C>G (p.Leu170Val) n.39C>G | |
19 | g.41348303G>T | CA406003463 | TGFB1 | c.508C>A (p.Leu170Met) n.39C>A | |
19 | g.41348304C>A | CA406003466 | TGFB1 | c.507G>T (p.Glu169Asp) n.38G>T | |
19 | g.41348304C>G | CA406003468 | TGFB1 | c.507G>C (p.Glu169Asp) n.38G>C | |
19 | g.41348304C>T | CA507555434 | TGFB1 | c.507G>A (p.Glu169=) n.38G>A | |
19 | g.41348305T>A | CA406003474 | TGFB1 | c.506A>T (p.Glu169Val) n.37A>T | |
19 | g.41348305T>C | CA406003472 | TGFB1 | c.506A>G (p.Glu169Gly) n.37A>G | |
19 | g.41348305T>G | CA406003470 | TGFB1 | c.506A>C (p.Glu169Ala) n.37A>C | |
19 | g.41348306C>A | CA406003475 | TGFB1 | c.505G>T (p.Glu169Ter) n.36G>T | |
19 | g.41348306C= | CA2336423944 | TGFB1 | c.505G= (p.Glu169=) n.36G= | |
19 | g.41348306C>G | CA9460083 | TGFB1 | c.505G>C (p.Glu169Gln) n.36G>C | ClinVar dbSNP ExAC gnomAD v4 |
19 | g.41348306C>T | CA308515302 | TGFB1 | c.505G>A (p.Glu169Lys) n.36G>A | dbSNP |
19 | g.41348307C>A | CA507555436 | TGFB1 | c.504G>T (p.Val168=) n.35G>T | |
19 | g.41348307C= | CA2336423945 | TGFB1 | c.504G= (p.Val168=) n.35G= | |
19 | g.41348307C>G | CA507555438 | TGFB1 | c.504G>C (p.Val168=) n.35G>C | |
19 | g.41348307C>T | CA507555439 | TGFB1 | c.504G>A (p.Val168=) n.35G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.41348308A>C | CA406003478 | TGFB1 | c.503T>G (p.Val168Gly) n.34T>G | |
19 | g.41348308A>G | CA406003479 | TGFB1 | c.503T>C (p.Val168Ala) n.34T>C | |
19 | g.41348308A>T | CA406003486 | TGFB1 | c.503T>A (p.Val168Glu) n.34T>A | |
19 | g.41348309C>A | CA406003489 | TGFB1 | c.502G>T (p.Val168Leu) n.33G>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.41348309C= | CA2336423946 | TGFB1 | c.502G= (p.Val168=) n.33G= | |
19 | g.41348309C>G | CA406003491 | TGFB1 | c.502G>C (p.Val168Leu) n.33G>C | |
19 | g.41348309C>T | CA406003494 | TGFB1 | c.502G>A (p.Val168Met) n.33G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348310G>A | CA9460084 | TGFB1 | c.501C>T (p.His167=) n.32C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348310G>C | CA406003495 | TGFB1 | c.501C>G (p.His167Gln) n.32C>G | gnomAD v4 |
19 | g.41348310G= | CA2336423947 | TGFB1 | c.501C= (p.His167=) n.32C= | |
19 | g.41348310G>T | CA406003496 | TGFB1 | c.501C>A (p.His167Gln) n.32C>A | |
19 | g.41348311T>A | CA406003498 | TGFB1 | c.500A>T (p.His167Leu) n.31A>T | |
19 | g.41348311T>C | CA406003499 | TGFB1 | c.500A>G (p.His167Arg) n.31A>G | |
19 | g.41348311T>G | CA406003497 | TGFB1 | c.500A>C (p.His167Pro) n.31A>C | |
19 | g.41348312G>A | CA406003500 | TGFB1 | c.499C>T (p.His167Tyr) n.30C>T | gnomAD v4 |
19 | g.41348312G>C | CA406003501 | TGFB1 | c.499C>G (p.His167Asp) n.30C>G | ClinVar gnomAD v4 |
19 | g.41348312G>T | CA406003503 | TGFB1 | c.499C>A (p.His167Asn) n.30C>A | |
19 | g.41348313C>A | CA406003506 | TGFB1 | c.498G>T (p.Gln166His) n.29G>T | |
19 | g.41348313C>G | CA406003509 | TGFB1 | c.498G>C (p.Gln166His) n.29G>C | |
19 | g.41348313C>T | CA507555446 | TGFB1 | c.498G>A (p.Gln166=) n.29G>A | |
19 | g.41348314T>A | CA406003514 | TGFB1 | c.497A>T (p.Gln166Leu) n.28A>T | |
19 | g.41348314T>C | CA406003512 | TGFB1 | c.497A>G (p.Gln166Arg) n.28A>G | |
19 | g.41348314T>G | CA406003513 | TGFB1 | c.497A>C (p.Gln166Pro) n.28A>C | gnomAD v4 |
19 | g.41348315G>A | CA406003516 | TGFB1 | c.496C>T (p.Gln166Ter) n.27C>T | dbSNP gnomAD v2 gnomAD v4 |
19 | g.41348315G>C | CA406003517 | TGFB1 | c.496C>G (p.Gln166Glu) n.27C>G | |
19 | g.41348315G= | CA2336423948 | TGFB1 | c.496C= (p.Gln166=) n.27C= | |
19 | g.41348315G>T | CA406003518 | TGFB1 | c.496C>A (p.Gln166Lys) n.27C>A | |
19 | g.41348316C>A | CA406003519 | TGFB1 | c.495G>T (p.Glu165Asp) n.26G>T | |
19 | g.41348316C>G | CA406003523 | TGFB1 | c.495G>C (p.Glu165Asp) n.26G>C | |
19 | g.41348316C>T | CA507555450 | TGFB1 | c.495G>A (p.Glu165=) n.26G>A | |
19 | g.41348317T>A | CA406003525 | TGFB1 | c.494A>T (p.Glu165Val) n.25A>T | |
19 | g.41348317T>C | CA406003528 | TGFB1 | c.494A>G (p.Glu165Gly) n.25A>G | |
19 | g.41348317T>G | CA406003527 | TGFB1 | c.494A>C (p.Glu165Ala) n.25A>C | |
19 | g.41348318C>A | CA406003530 | TGFB1 | c.493G>T (p.Glu165Ter) n.24G>T | |
19 | g.41348318C>G | CA406003531 | TGFB1 | c.493G>C (p.Glu165Gln) n.24G>C | |
19 | g.41348318C>T | CA406003532 | TGFB1 | c.493G>A (p.Glu165Lys) n.24G>A | |
19 | g.41348319C>A | CA507555455 | TGFB1 | c.492G>T (p.Val164=) n.23G>T | |
19 | g.41348319C>G | CA507555456 | TGFB1 | c.492G>C (p.Val164=) n.23G>C | |
19 | g.41348319C>T | CA507555457 | TGFB1 | c.492G>A (p.Val164=) n.23G>A | ClinVar dbSNP |
19 | g.41348320A>C | CA406003533 | TGFB1 | c.491T>G (p.Val164Gly) n.22T>G | |
19 | g.41348320A>G | CA406003539 | TGFB1 | c.491T>C (p.Val164Ala) n.22T>C | |
19 | g.41348320A>T | CA406003540 | TGFB1 | c.491T>A (p.Val164Glu) n.22T>A | |
19 | g.41348321C>A | CA406003543 | TGFB1 | c.490G>T (p.Val164Leu) n.21G>T | |
19 | g.41348321C>G | CA406003545 | TGFB1 | c.490G>C (p.Val164Leu) n.21G>C | |
19 | g.41348321C>T | CA406003546 | TGFB1 | c.490G>A (p.Val164Met) n.21G>A | |
19 | g.41348322T>A | CA406003548 | TGFB1 | c.489A>T (p.Lys163Asn) n.20A>T | |
19 | g.41348322T>C | CA507555460 | TGFB1 | c.489A>G (p.Lys163=) n.20A>G | |
19 | g.41348322T>G | CA406003550 | TGFB1 | c.489A>C (p.Lys163Asn) n.20A>C | gnomAD v4 |
19 | g.41348325dup | CA2840843134 | TGFB1 | c.489dup (p.Val164SerfsTer?) n.20dup | |
19 | g.41348323T>A | CA406003555 | TGFB1 | c.488A>T (p.Lys163Ile) n.19A>T | gnomAD v4 |
19 | g.41348323T>C | CA406003553 | TGFB1 | c.488A>G (p.Lys163Arg) n.19A>G | |
19 | g.41348323T>G | CA406003552 | TGFB1 | c.488A>C (p.Lys163Thr) n.19A>C | |
19 | g.41348324T>A | CA406003557 | TGFB1 | c.487A>T (p.Lys163Ter) n.18A>T | |
19 | g.41348324T>C | CA406003561 | TGFB1 | c.487A>G (p.Lys163Glu) n.18A>G | |
19 | g.41348324T>G | CA406003559 | TGFB1 | c.487A>C (p.Lys163Gln) n.18A>C | |
19 | g.41348325T>A | CA406003563 | TGFB1 | c.486A>T (p.Leu162Phe) n.17A>T | |
19 | g.41348325T>C | CA507555466 | TGFB1 | c.486A>G (p.Leu162=) n.17A>G | |
19 | g.41348325T>G | CA406003565 | TGFB1 | c.486A>C (p.Leu162Phe) n.17A>C | |
19 | g.41348326A>C | CA406003566 | TGFB1 | c.485T>G (p.Leu162Ter) n.16T>G | |
19 | g.41348326A>G | CA406003567 | TGFB1 | c.485T>C (p.Leu162Ser) n.16T>C | ClinVar |
19 | g.41348326A>T | CA406003568 | TGFB1 | c.485T>A (p.Leu162Ter) n.16T>A | |
19 | g.41348327A>C | CA406003569 | TGFB1 | c.484T>G (p.Leu162Val) n.15T>G | |
19 | g.41348327A>G | CA507555467 | TGFB1 | c.484T>C (p.Leu162=) n.15T>C | |
19 | g.41348327A>T | CA406003570 | TGFB1 | c.484T>A (p.Leu162Ile) n.15T>A | |
19 | g.41348328C>A | CA406003571 | TGFB1 | c.483G>T (p.Lys161Asn) n.14G>T | ClinVar |
19 | g.41348328C>G | CA406003572 | TGFB1 | c.483G>C (p.Lys161Asn) n.14G>C | |
19 | g.41348328C>T | CA507555471 | TGFB1 | c.483G>A (p.Lys161=) n.14G>A | |
19 | g.41348329T>A | CA406003573 | TGFB1 | c.482A>T (p.Lys161Met) n.13A>T | |
19 | g.41348329T>C | CA406003574 | TGFB1 | c.482A>G (p.Lys161Arg) n.13A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
19 | g.41348329T>G | CA406003575 | TGFB1 | c.482A>C (p.Lys161Thr) n.13A>C | gnomAD v4 |
19 | g.41348329T= | CA2336423949 | TGFB1 | c.482A= (p.Lys161=) n.13A= | |
19 | g.41348330T>A | CA406003578 | TGFB1 | c.481A>T (p.Lys161Ter) n.12A>T | |
19 | g.41348330T>C | CA406003576 | TGFB1 | c.481A>G (p.Lys161Glu) n.12A>G | |
19 | g.41348330T>G | CA406003577 | TGFB1 | c.481A>C (p.Lys161Gln) n.12A>C | |
19 | g.41348330_41348332del | CA2585296893 | TGFB1 | c.479_481del (p.Leu160_Lys161delinsGln) n.10_12del | gnomAD v4 |
19 | g.41348331G>A | CA507555473 | TGFB1 | c.480C>T (p.Leu160=) n.11C>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.41348331G>C | CA507555474 | TGFB1 | c.480C>G (p.Leu160=) n.11C>G | |
19 | g.41348331G= | CA2336423950 | TGFB1 | c.480C= (p.Leu160=) n.11C= | |
19 | g.41348331G>T | CA507555476 | TGFB1 | c.480C>A (p.Leu160=) n.11C>A | |
19 | g.41348332A>C | CA406003579 | TGFB1 | c.479T>G (p.Leu160Arg) n.10T>G | |
19 | g.41348332A>G | CA406003580 | TGFB1 | c.479T>C (p.Leu160Pro) n.10T>C | |
19 | g.41348332A>T | CA406003581 | TGFB1 | c.479T>A (p.Leu160His) n.10T>A | |
19 | g.41348333G>A | CA308515312 | TGFB1 | c.478C>T (p.Leu160Phe) n.9C>T | dbSNP gnomAD v4 |
19 | g.41348333G>C | CA406003582 | TGFB1 | c.478C>G (p.Leu160Val) n.9C>G | |
19 | g.41348333G= | CA2336423951 | TGFB1 | c.478C= (p.Leu160=) n.9C= | |
19 | g.41348333G>T | CA406003583 | TGFB1 | c.478C>A (p.Leu160Ile) n.9C>A | |
19 | g.41348334C>A | CA406003584 | TGFB1 | c.477G>T (p.Arg159Ser) n.8G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348334C= | CA2336423952 | TGFB1 | c.477G= (p.Arg159=) n.8G= | |
19 | g.41348334C>G | CA406003585 | TGFB1 | c.477G>C (p.Arg159Ser) n.8G>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.41348334C>T | CA507555479 | TGFB1 | c.477G>A (p.Arg159=) n.8G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348335C>A | CA406003586 | TGFB1 | c.476G>T (p.Arg159Met) n.7G>T | |
19 | g.41348335C>G | CA406003587 | TGFB1 | c.476G>C (p.Arg159Thr) n.7G>C | |
19 | g.41348335C>T | CA406003588 | TGFB1 | c.476G>A (p.Arg159Lys) n.7G>A | |
19 | g.41348336T>A | CA406003589 | TGFB1 | c.475A>T (p.Arg159Trp) n.6A>T | |
19 | g.41348336T>C | CA406003590 | TGFB1 | c.475A>G (p.Arg159Gly) n.6A>G | |
19 | g.41348336T>G | CA507555483 | TGFB1 | c.475A>C (p.Arg159=) n.6A>C | |
19 | g.41348337C>A | CA507555484 | TGFB1 | c.474G>T (p.Leu158=) n.5G>T | |
19 | g.41348337C= | CA2336423953 | TGFB1 | c.474G= (p.Leu158=) n.5G= | |
19 | g.41348337C>G | CA507555485 | TGFB1 | c.474G>C (p.Leu158=) n.5G>C | |
19 | g.41348337C>T | CA9460085 | TGFB1 | c.474G>A (p.Leu158=) n.5G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348338A>C | CA406003591 | TGFB1 | c.473T>G (p.Leu158Arg) n.4T>G | |
19 | g.41348338A>G | CA406003592 | TGFB1 | c.473T>C (p.Leu158Pro) n.4T>C | COSMIC |
19 | g.41348338A>T | CA406003593 | TGFB1 | c.473T>A (p.Leu158Gln) n.4T>A | |
19 | g.41348339G>A | CA507555488 | TGFB1 | c.472C>T (p.Leu158=) n.3C>T | |
19 | g.41348339G>C | CA406003594 | TGFB1 | c.472C>G (p.Leu158Val) n.3C>G | |
19 | g.41348339G>T | CA406003595 | TGFB1 | c.472C>A (p.Leu158Met) n.3C>A | |
19 | g.41348340C>A | CA507555489 | TGFB1 | c.471G>T (p.Leu157=) n.2G>T | |
19 | g.41348340C>G | CA507555490 | TGFB1 | c.471G>C (p.Leu157=) n.2G>C | |
19 | g.41348340C>T | CA507555491 | TGFB1 | c.471G>A (p.Leu157=) n.2G>A | |
19 | g.41348341A>C | CA406003598 | TGFB1 | c.470T>G (p.Leu157Arg) n.1T>G | |
19 | g.41348341A>G | CA406003596 | TGFB1 | c.470T>C (p.Leu157Pro) n.1T>C | |
19 | g.41348341A>T | CA406003597 | TGFB1 | c.470T>A (p.Leu157Gln) n.1T>A | |
19 | g.41348342G>A | CA507555494 | TGFB1 | c.469C>T (p.Leu157=) | |
19 | g.41348342G>C | CA406003599 | TGFB1 | c.469C>G (p.Leu157Val) | |
19 | g.41348342G>T | CA406003600 | TGFB1 | c.469C>A (p.Leu157Met) | |
19 | g.41348343A>C | CA507555495 | TGFB1 | c.468T>G (p.Arg156=) | gnomAD v4 |
19 | g.41348343A>G | CA507555496 | TGFB1 | c.468T>C (p.Arg156=) | |
19 | g.41348343A>T | CA507555497 | TGFB1 | c.468T>A (p.Arg156=) | |
19 | g.41348344C>A | CA406003601 | TGFB1 | c.467G>T (p.Arg156Leu) | |
19 | g.41348344C>G | CA406003602 | TGFB1 | c.467G>C (p.Arg156Pro) | |
19 | g.41348344C>T | CA406003603 | TGFB1 | c.467G>A (p.Arg156His) | ClinVar gnomAD v4 COSMIC |
19 | g.41348345G>A | CA308515324 | TGFB1 | c.466C>T (p.Arg156Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
19 | g.41348345G>C | CA406003605 | TGFB1 | c.466C>G (p.Arg156Gly) | |
19 | g.41348345G= | CA2336423954 | TGFB1 | c.466C= (p.Arg156=) | |
19 | g.41348345G>T | CA406003604 | TGFB1 | c.466C>A (p.Arg156Ser) | gnomAD v4 |
19 | g.41348346C>A | CA507555501 | TGFB1 | c.465G>T (p.Leu155=) | |
19 | g.41348346C>G | CA507555502 | TGFB1 | c.465G>C (p.Leu155=) | |
19 | g.41348346C>T | CA507555504 | TGFB1 | c.465G>A (p.Leu155=) | |
19 | g.41348347A>C | CA406003606 | TGFB1 | c.464T>G (p.Leu155Arg) | |
19 | g.41348347A>G | CA406003607 | TGFB1 | c.464T>C (p.Leu155Pro) | |
19 | g.41348347A>T | CA406003608 | TGFB1 | c.464T>A (p.Leu155Gln) | |
19 | g.41348348G>A | CA507555507 | TGFB1 | c.463C>T (p.Leu155=) | dbSNP gnomAD v4 |
19 | g.41348348G>C | CA406003609 | TGFB1 | c.463C>G (p.Leu155Val) | |
19 | g.41348348G= | CA2336423955 | TGFB1 | c.463C= (p.Leu155=) | |
19 | g.41348348G>T | CA406003610 | TGFB1 | c.463C>A (p.Leu155Met) | |
19 | g.41348349C>A | CA406003611 | TGFB1 | c.462G>T (p.Glu154Asp) | |
19 | g.41348349C= | CA2336423956 | TGFB1 | c.462G= (p.Glu154=) | |
19 | g.41348349C>G | CA406003612 | TGFB1 | c.462G>C (p.Glu154Asp) | |
19 | g.41348349C>T | CA507555510 | TGFB1 | c.462G>A (p.Glu154=) | dbSNP |
19 | g.41348350T>A | CA406003613 | TGFB1 | c.461A>T (p.Glu154Val) | |
19 | g.41348350T>C | CA406003614 | TGFB1 | c.461A>G (p.Glu154Gly) | |
19 | g.41348350T>G | CA406003615 | TGFB1 | c.461A>C (p.Glu154Ala) | |
19 | g.41348351C>A | CA406003617 | TGFB1 | c.460G>T (p.Glu154Ter) | |
19 | g.41348351C= | CA2336423957 | TGFB1 | c.460G= (p.Glu154=) | |
19 | g.41348351C>G | CA406003616 | TGFB1 | c.460G>C (p.Glu154Gln) | |
19 | g.41348351C>T | CA308515334 | TGFB1 | c.460G>A (p.Glu154Lys) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.41348352T>A | CA507555512 | TGFB1 | c.459A>T (p.Ala153=) | |
19 | g.41348352T>C | CA507555513 | TGFB1 | c.459A>G (p.Ala153=) | dbSNP |
19 | g.41348352T>G | CA507555514 | TGFB1 | c.459A>C (p.Ala153=) | |
19 | g.41348352T= | CA2336423958 | TGFB1 | c.459A= (p.Ala153=) | |
19 | g.41348353G>A | CA406003618 | TGFB1 | c.458C>T (p.Ala153Val) | |
19 | g.41348353G>C | CA406003620 | TGFB1 | c.458C>G (p.Ala153Gly) | |
19 | g.41348353G>T | CA406003619 | TGFB1 | c.458C>A (p.Ala153Glu) | gnomAD v4 |
19 | g.41348354C>A | CA406003621 | TGFB1 | c.457G>T (p.Ala153Ser) | |
19 | g.41348354C= | CA2336423959 | TGFB1 | c.457G= (p.Ala153=) | |
19 | g.41348354C>G | CA406003623 | TGFB1 | c.457G>C (p.Ala153Pro) | |
19 | g.41348354C>T | CA406003622 | TGFB1 | c.457G>A (p.Ala153Thr) | dbSNP |
19 | g.41348355C>A | CA507555517 | TGFB1 | c.456G>T (p.Arg152=) | |
19 | g.41348355C= | CA2336423960 | TGFB1 | c.456G= (p.Arg152=) | |
19 | g.41348355C>G | CA507555519 | TGFB1 | c.456G>C (p.Arg152=) | |
19 | g.41348355C>T | CA9460086 | TGFB1 | c.456G>A (p.Arg152=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
19 | g.41348356C>A | CA9460088 | TGFB1 | c.455G>T (p.Arg152Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.41348356C= | CA2336423961 | TGFB1 | c.455G= (p.Arg152=) | |
19 | g.41348356C>G | CA406003624 | TGFB1 | c.455G>C (p.Arg152Pro) | |
19 | g.41348356C>T | CA9460087 | TGFB1 | c.455G>A (p.Arg152Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348357G>A | CA9460089 | TGFB1 | c.454C>T (p.Arg152Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348357G>C | CA406003625 | TGFB1 | c.454C>G (p.Arg152Gly) | |
19 | g.41348357G= | CA2336423962 | TGFB1 | c.454C= (p.Arg152=) | |
19 | g.41348357G>T | CA507555521 | TGFB1 | c.454C>A (p.Arg152=) | |
19 | g.41348359dup | CA2839696004 | TGFB1 | c.454dup (p.Arg152ProfsTer?) | |
19 | g.41348358G>A | CA507555523 | TGFB1 | c.453C>T (p.Ser151=) | |
19 | g.41348358G>C | CA507555525 | TGFB1 | c.453C>G (p.Ser151=) | |
19 | g.41348358G>T | CA507555528 | TGFB1 | c.453C>A (p.Ser151=) | |
19 | g.41348359G>A | CA9460090 | TGFB1 | c.452C>T (p.Ser151Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348359G>C | CA406003626 | TGFB1 | c.452C>G (p.Ser151Cys) | |
19 | g.41348359G= | CA2336423963 | TGFB1 | c.452C= (p.Ser151=) | |
19 | g.41348359G>T | CA406003627 | TGFB1 | c.452C>A (p.Ser151Tyr) | |
19 | g.41348360A>C | CA406003628 | TGFB1 | c.451T>G (p.Ser151Ala) | |
19 | g.41348360A>G | CA406003629 | TGFB1 | c.451T>C (p.Ser151Pro) | |
19 | g.41348360A>T | CA406003630 | TGFB1 | c.451T>A (p.Ser151Thr) | |
19 | g.41348361G>A | CA507555529 | TGFB1 | c.450C>T (p.Leu150=) | |
19 | g.41348361G>C | CA507555530 | TGFB1 | c.450C>G (p.Leu150=) | |
19 | g.41348361G>T | CA507555532 | TGFB1 | c.450C>A (p.Leu150=) | |
19 | g.41348362A>C | CA406003631 | TGFB1 | c.449T>G (p.Leu150Arg) | |
19 | g.41348362A>G | CA406003633 | TGFB1 | c.449T>C (p.Leu150Pro) | |
19 | g.41348362A>T | CA406003632 | TGFB1 | c.449T>A (p.Leu150His) | |
19 | g.41348363G>A | CA406003634 | TGFB1 | c.448C>T (p.Leu150Phe) | |
19 | g.41348363G>C | CA406003635 | TGFB1 | c.448C>G (p.Leu150Val) | |
19 | g.41348363G>T | CA406003636 | TGFB1 | c.448C>A (p.Leu150Ile) | |
19 | g.41348364C>A | CA406003637 | TGFB1 | c.447G>T (p.Leu149Phe) | |
19 | g.41348364C>G | CA406003638 | TGFB1 | c.447G>C (p.Leu149Phe) | |
19 | g.41348364C>T | CA507555535 | TGFB1 | c.447G>A (p.Leu149=) | |
19 | g.41348365A>C | CA406003639 | TGFB1 | c.446T>G (p.Leu149Trp) | |
19 | g.41348365A>G | CA406003640 | TGFB1 | c.446T>C (p.Leu149Ser) | |
19 | g.41348365A>T | CA406003641 | TGFB1 | c.446T>A (p.Leu149Ter) | |
19 | g.41348366A>C | CA406003642 | TGFB1 | c.445T>G (p.Leu149Val) | |
19 | g.41348366A>G | CA507555538 | TGFB1 | c.445T>C (p.Leu149=) | gnomAD v4 |
19 | g.41348366A>T | CA406003643 | TGFB1 | c.445T>A (p.Leu149Met) | |
19 | g.41348367C>A | CA507555539 | TGFB1 | c.444G>T (p.Val148=) | gnomAD v4 |
19 | g.41348367C>G | CA507555542 | TGFB1 | c.444G>C (p.Val148=) | |
19 | g.41348367C>T | CA507555541 | TGFB1 | c.444G>A (p.Val148=) | |
19 | g.41348368A= | CA2336423964 | TGFB1 | c.443T= (p.Val148=) | |
19 | g.41348368A>C | CA406003645 | TGFB1 | c.443T>G (p.Val148Gly) | |
19 | g.41348368A>G | CA9460091 | TGFB1 | c.443T>C (p.Val148Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.41348368A>T | CA406003644 | TGFB1 | c.443T>A (p.Val148Glu) | |
19 | g.41348369C>A | CA9460093 | TGFB1 | c.442G>T (p.Val148Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.41348369C= | CA2336423965 | TGFB1 | c.442G= (p.Val148=) | |
19 | g.41348369C>G | CA406003646 | TGFB1 | c.442G>C (p.Val148Leu) | gnomAD v4 |
19 | g.41348369C>T | CA9460092 | TGFB1 | c.442G>A (p.Val148Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348370G>A | CA9460094 | TGFB1 | c.441C>T (p.Pro147=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348370G>C | CA308515364 | TGFB1 | c.441C>G (p.Pro147=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348370G= | CA2336423966 | TGFB1 | c.441C= (p.Pro147=) | |
19 | g.41348370G>T | CA507555544 | TGFB1 | c.441C>A (p.Pro147=) | |
19 | g.41348372del | CA2697556593 | TGFB1 | c.441del (p.Val148CysfsTer11) | ClinVar |
19 | g.41348371G>A | CA406003647 | TGFB1 | c.440C>T (p.Pro147Leu) | |
19 | g.41348371G>C | CA406003648 | TGFB1 | c.440C>G (p.Pro147Arg) | |
19 | g.41348371G>T | CA406003649 | TGFB1 | c.440C>A (p.Pro147His) | |
19 | g.41348372G>A | CA406003650 | TGFB1 | c.439C>T (p.Pro147Ser) | dbSNP gnomAD v2 |
19 | g.41348372G>C | CA406003651 | TGFB1 | c.439C>G (p.Pro147Ala) | |
19 | g.41348372G= | CA2336423967 | TGFB1 | c.439C= (p.Pro147=) | |
19 | g.41348372G>T | CA406003652 | TGFB1 | c.439C>A (p.Pro147Thr) | |
19 | g.41348373T>A | CA406003653 | TGFB1 | c.438A>T (p.Glu146Asp) | |
19 | g.41348373T>C | CA507555549 | TGFB1 | c.438A>G (p.Glu146=) | |
19 | g.41348373T>G | CA406003654 | TGFB1 | c.438A>C (p.Glu146Asp) | |
19 | g.41348374T>A | CA406003657 | TGFB1 | c.437A>T (p.Glu146Val) | |
19 | g.41348374T>C | CA406003656 | TGFB1 | c.437A>G (p.Glu146Gly) | |
19 | g.41348374T>G | CA406003655 | TGFB1 | c.437A>C (p.Glu146Ala) | |
19 | g.41348375C>A | CA406003658 | TGFB1 | c.436G>T (p.Glu146Ter) | |
19 | g.41348375C= | CA2336423968 | TGFB1 | c.436G= (p.Glu146=) | |
19 | g.41348375C>G | CA308515368 | TGFB1 | c.436G>C (p.Glu146Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41348375C>T | CA406003659 | TGFB1 | c.436G>A (p.Glu146Lys) | |
19 | g.41348376A= | CA2336423969 | TGFB1 | c.435T= (p.Pro145=) | |
19 | g.41348376A>C | CA9460095 | TGFB1 | c.435T>G (p.Pro145=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.41348376A>G | CA507555551 | TGFB1 | c.435T>C (p.Pro145=) | gnomAD v4 |
19 | g.41348376A>T | CA507555552 | TGFB1 | c.435T>A (p.Pro145=) |