| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.41348223C>A | CA2576793315 | TGFB1 | c.516+72G>T (n.516+72G>T) n.47+72G>T | gnomAD v4 |
| 19 | g.41348223C>T | CA2565061375 | TGFB1 | c.516+72G>A (n.516+72G>A) n.47+72G>A | gnomAD v4 |
| 19 | g.41348224A>G | CA2585296861 | TGFB1 | c.516+71T>C (n.516+71T>C) n.47+71T>C | gnomAD v4 |
| 19 | g.41348224A>T | CA2585296862 | TGFB1 | c.516+71T>A (n.516+71T>A) n.47+71T>A | gnomAD v4 |
| 19 | g.41348225G>A | CA2336423910 | TGFB1 | c.516+70C>T (n.516+70C>T) n.47+70C>T | dbSNP |
| 19 | g.41348225G= | CA2336423909 | TGFB1 | c.516+70C= (n.516+70C=) n.47+70C= | |
| 19 | g.41348225G>T | CA2585296863 | TGFB1 | c.516+70C>A (n.516+70C>A) n.47+70C>A | gnomAD v4 |
| 19 | g.41348226C>A | CA2585296864 | TGFB1 | c.516+69G>T (n.516+69G>T) n.47+69G>T | gnomAD v4 |
| 19 | g.41348226C>G | CA2585296865 | TGFB1 | c.516+69G>C (n.516+69G>C) n.47+69G>C | gnomAD v4 |
| 19 | g.41348226C>T | CA2585296866 | TGFB1 | c.516+69G>A (n.516+69G>A) n.47+69G>A | gnomAD v4 |
| 19 | g.41348227C>A | CA2585296867 | TGFB1 | c.516+68G>T (n.516+68G>T) n.47+68G>T | gnomAD v4 |
| 19 | g.41348227C>T | CA657412159 | TGFB1 | c.516+68G>A (n.516+68G>A) n.47+68G>A | COSMIC |
| 19 | g.41348228_41348229delinsAC | CA2336423911 | TGFB1 | c.516+66_516+67delinsGT (n.516+66_516+67delinsGT) n.47+66_47+67delinsGT | |
| 19 | g.41348229C>A | CA308515246 | TGFB1 | c.516+66G>T (n.516+66G>T) n.47+66G>T | dbSNP gnomAD v4 |
| 19 | g.41348229C= | CA2336423913 | TGFB1 | c.516+66G= (n.516+66G=) n.47+66G= | |
| 19 | g.41348229C>T | CA882319732 | TGFB1 | c.516+66G>A (n.516+66G>A) n.47+66G>A | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.41348233dup | CA2576793316 | TGFB1 | c.516+66dup (n.516+66dup) n.47+66dup | |
| 19 | g.41348233del | CA2336423912 | TGFB1 | c.516+66del (n.516+66del) n.47+66del | dbSNP gnomAD v4 |
| 19 | g.41348230C>A | CA633167499 | TGFB1 | c.516+65G>T (n.516+65G>T) n.47+65G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.41348230C= | CA2336423914 | TGFB1 | c.516+65G= (n.516+65G=) n.47+65G= | |
| 19 | g.41348230C>T | CA995961145 | TGFB1 | c.516+65G>A (n.516+65G>A) n.47+65G>A | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.41348231C>A | CA2585296868 | TGFB1 | c.516+64G>T (n.516+64G>T) n.47+64G>T | gnomAD v4 |
| 19 | g.41348231C= | CA2336423915 | TGFB1 | c.516+64G= (n.516+64G=) n.47+64G= | |
| 19 | g.41348231C>T | CA633167500 | TGFB1 | c.516+64G>A (n.516+64G>A) n.47+64G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.41348232C>A | CA2585296869 | TGFB1 | c.516+63G>T (n.516+63G>T) n.47+63G>T | gnomAD v4 |
| 19 | g.41348232C= | CA2336423916 | TGFB1 | c.516+63G= (n.516+63G=) n.47+63G= | |
| 19 | g.41348232C>G | CA633167501 | TGFB1 | c.516+63G>C (n.516+63G>C) n.47+63G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.41348233C>G | CA2585296870 | TGFB1 | c.516+62G>C (n.516+62G>C) n.47+62G>C | gnomAD v4 |
| 19 | g.41348233C>T | CA2585296871 | TGFB1 | c.516+62G>A (n.516+62G>A) n.47+62G>A | gnomAD v4 |
| 19 | g.41348234T>A | CA633167502 | TGFB1 | c.516+61A>T (n.516+61A>T) n.47+61A>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.41348234T>C | CA2585296872 | TGFB1 | c.516+61A>G (n.516+61A>G) n.47+61A>G | dbSNP gnomAD v4 |
| 19 | g.41348234T>G | CA2576793317 | TGFB1 | c.516+61A>C (n.516+61A>C) n.47+61A>C | |
| 19 | g.41348234T= | CA2336423917 | TGFB1 | c.516+61A= (n.516+61A=) n.47+61A= | |
| 19 | g.41348235T>C | CA2585296873 | TGFB1 | c.516+60A>G (n.516+60A>G) n.47+60A>G | gnomAD v4 |
| 19 | g.41348236G>T | CA2585296874 | TGFB1 | c.516+59C>A (n.516+59C>A) n.47+59C>A | gnomAD v4 |
| 19 | g.41348237G>A | CA308515248 | TGFB1 | c.516+58C>T (n.516+58C>T) n.47+58C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.41348237G= | CA2336423918 | TGFB1 | c.516+58C= (n.516+58C=) n.47+58C= | |
| 19 | g.41348239C>A | CA2585296875 | TGFB1 | c.516+56G>T (n.516+56G>T) n.47+56G>T | gnomAD v4 |
| 19 | g.41348242_41348244dup | CA2585296876 | TGFB1 | c.516+52_516+54dup (n.516+52_516+54dup) n.47+52_47+54dup | gnomAD v4 |
| 19 | g.41348243G>A | CA2336423920 | TGFB1 | c.516+52C>T (n.516+52C>T) n.47+52C>T | dbSNP |
| 19 | g.41348243G= | CA2336423919 | TGFB1 | c.516+52C= (n.516+52C=) n.47+52C= | |
| 19 | g.41348243G>T | CA2576793318 | TGFB1 | c.516+52C>A (n.516+52C>A) n.47+52C>A | gnomAD v4 |
| 19 | g.41348244C>A | CA2585296877 | TGFB1 | c.516+51G>T (n.516+51G>T) n.47+51G>T | gnomAD v4 |
| 19 | g.41348244C= | CA2336423921 | TGFB1 | c.516+51G= (n.516+51G=) n.47+51G= | |
| 19 | g.41348244C>T | CA633167503 | TGFB1 | c.516+51G>A (n.516+51G>A) n.47+51G>A | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.41348245T>A | CA2585296878 | TGFB1 | c.516+50A>T (n.516+50A>T) n.47+50A>T | gnomAD v4 |
| 19 | g.41348247A>G | CA2576793319 | TGFB1 | c.516+48T>C (n.516+48T>C) n.47+48T>C | |
| 19 | g.41348248C>T | CA2585296879 | TGFB1 | c.516+47G>A (n.516+47G>A) n.47+47G>A | gnomAD v4 |
| 19 | g.41348249C= | CA2336423922 | TGFB1 | c.516+46G= (n.516+46G=) n.47+46G= | |
| 19 | g.41348249C>T | CA2336423923 | TGFB1 | c.516+46G>A (n.516+46G>A) n.47+46G>A | dbSNP |
| 19 | g.41348250C>G | CA2585296880 | TGFB1 | c.516+45G>C (n.516+45G>C) n.47+45G>C | gnomAD v4 |
| 19 | g.41348250C>T | CA2585296881 | TGFB1 | c.516+45G>A (n.516+45G>A) n.47+45G>A | gnomAD v4 |
| 19 | g.41348252C= | CA2336423924 | TGFB1 | c.516+43G= (n.516+43G=) n.47+43G= | |
| 19 | g.41348252C>T | CA9460078 | TGFB1 | c.516+43G>A (n.516+43G>A) n.47+43G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.41348255C= | CA2336423925 | TGFB1 | c.516+40G= (n.516+40G=) n.47+40G= | |
| 19 | g.41348255C>T | CA633167504 | TGFB1 | c.516+40G>A (n.516+40G>A) n.47+40G>A | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.41348257G>T | CA2585296882 | TGFB1 | c.516+38C>A (n.516+38C>A) n.47+38C>A | gnomAD v4 |
| 19 | g.41348258C>T | CA2585296884 | TGFB1 | c.516+37G>A (n.516+37G>A) n.47+37G>A | gnomAD v4 |
| 19 | g.41348260dup | CA2585296883 | TGFB1 | c.516+37dup (n.516+37dup) n.47+37dup | gnomAD v4 |
| 19 | g.41348259C>A | CA2585296885 | TGFB1 | c.516+36G>T (n.516+36G>T) n.47+36G>T | gnomAD v4 |
| 19 | g.41348259C>G | CA2585296886 | TGFB1 | c.516+36G>C (n.516+36G>C) n.47+36G>C | gnomAD v4 |
| 19 | g.41348259C>T | CA2585296887 | TGFB1 | c.516+36G>A (n.516+36G>A) n.47+36G>A | gnomAD v4 |
| 19 | g.41348260C>T | CA2576793320 | TGFB1 | c.516+35G>A (n.516+35G>A) n.47+35G>A | gnomAD v4 |
| 19 | g.41348262T>C | CA2585296888 | TGFB1 | c.516+33A>G (n.516+33A>G) n.47+33A>G | gnomAD v4 |
| 19 | g.41348263G>A | CA633167505 | TGFB1 | c.516+32C>T (n.516+32C>T) n.47+32C>T | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.41348263G= | CA2336423926 | TGFB1 | c.516+32C= (n.516+32C=) n.47+32C= | |
| 19 | g.41348265C>A | CA308515251 | TGFB1 | c.516+30G>T (n.516+30G>T) n.47+30G>T | dbSNP |
| 19 | g.41348265C= | CA2336423927 | TGFB1 | c.516+30G= (n.516+30G=) n.47+30G= | |
| 19 | g.41348270C>A | CA633167506 | TGFB1 | c.516+25G>T (n.516+25G>T) n.47+25G>T | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.41348270C= | CA2336423928 | TGFB1 | c.516+25G= (n.516+25G=) n.47+25G= | |
| 19 | g.41348275C>A | CA2336423930 | TGFB1 | c.516+20G>T (n.516+20G>T) n.47+20G>T | dbSNP |
| 19 | g.41348275C= | CA2336423929 | TGFB1 | c.516+20G= (n.516+20G=) n.47+20G= | |
| 19 | g.41348275C>T | CA2585296889 | TGFB1 | c.516+20G>A (n.516+20G>A) n.47+20G>A | gnomAD v4 |
| 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.41348281G>A | CA2573156383 | TGFB1 | c.516+14C>T (n.516+14C>T) n.47+14C>T | ClinVar dbSNP gnomAD v4 |
| 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.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= | 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.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 |