Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.81729549T>C | CA2683531183 | HGF | c.1040+56A>G (n.1040+56A>G) c.1025+56A>G (n.1025+56A>G) | gnomAD v4 |
7 | g.81729550A>C | CA2683531184 | HGF | c.1040+55T>G (n.1040+55T>G) c.1025+55T>G (n.1025+55T>G) | gnomAD v4 |
7 | g.81729550A>T | CA2715096605 | HGF | c.1040+55T>A (n.1040+55T>A) c.1025+55T>A (n.1025+55T>A) | dbSNP |
7 | g.81729552C>A | CA2841934988 | HGF | c.1040+53G>T (n.1040+53G>T) c.1025+53G>T (n.1025+53G>T) | |
7 | g.81729552C= | CA1720888208 | HGF | c.1040+53G= (n.1040+53G=) c.1025+53G= (n.1025+53G=) | |
7 | g.81729552C>T | CA1720888209 | HGF | c.1040+53G>A (n.1040+53G>A) c.1025+53G>A (n.1025+53G>A) | dbSNP gnomAD v4 |
7 | g.81729555A= | CA1720888210 | HGF | c.1040+50T= (n.1040+50T=) c.1025+50T= (n.1025+50T=) | |
7 | g.81729555A>G | CA2683531185 | HGF | c.1040+50T>C (n.1040+50T>C) c.1025+50T>C (n.1025+50T>C) | gnomAD v4 |
7 | g.81729555A>T | CA1720888211 | HGF | c.1040+50T>A (n.1040+50T>A) c.1025+50T>A (n.1025+50T>A) | dbSNP |
7 | g.81729556T>C | CA2578923860 | HGF | c.1040+49A>G (n.1040+49A>G) c.1025+49A>G (n.1025+49A>G) | |
7 | g.81729559del | CA2683531186 | HGF | c.1040+49del (n.1040+49del) c.1025+49del (n.1025+49del) | dbSNP gnomAD v4 |
7 | g.81729559T>A | CA2683531187 | HGF | c.1040+46A>T (n.1040+46A>T) c.1025+46A>T (n.1025+46A>T) | gnomAD v4 |
7 | g.81729559T>C | CA2578923861 | HGF | c.1040+46A>G (n.1040+46A>G) c.1025+46A>G (n.1025+46A>G) | |
7 | g.81729560C>A | CA2683531189 | HGF | c.1040+45G>T (n.1040+45G>T) c.1025+45G>T (n.1025+45G>T) | gnomAD v4 |
7 | g.81729560C= | CA1720888212 | HGF | c.1040+45G= (n.1040+45G=) c.1025+45G= (n.1025+45G=) | |
7 | g.81729560C>T | CA4316998 | HGF | c.1040+45G>A (n.1040+45G>A) c.1025+45G>A (n.1025+45G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.81729563del | CA2683531188 | HGF | c.1040+45del (n.1040+45del) c.1025+45del (n.1025+45del) | gnomAD v4 |
7 | g.81729561C= | CA1720888213 | HGF | c.1040+44G= (n.1040+44G=) c.1025+44G= (n.1025+44G=) | |
7 | g.81729561C>T | CA4316999 | HGF | c.1040+44G>A (n.1040+44G>A) c.1025+44G>A (n.1025+44G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.81729562C>A | CA2683531190 | HGF | c.1040+43G>T (n.1040+43G>T) c.1025+43G>T (n.1025+43G>T) | gnomAD v4 |
7 | g.81729563C>A | CA2715096610 | HGF | c.1040+42G>T (n.1040+42G>T) c.1025+42G>T (n.1025+42G>T) | dbSNP |
7 | g.81729565G>A | CA4317000 | HGF | c.1040+40C>T (n.1040+40C>T) c.1025+40C>T (n.1025+40C>T) | dbSNP ExAC gnomAD v4 |
7 | g.81729565G= | CA1720888214 | HGF | c.1040+40C= (n.1040+40C=) c.1025+40C= (n.1025+40C=) | |
7 | g.81729565G>T | CA575808881 | HGF | c.1040+40C>A (n.1040+40C>A) c.1025+40C>A (n.1025+40C>A) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729566G>T | CA2683531191 | HGF | c.1040+39C>A (n.1040+39C>A) c.1025+39C>A (n.1025+39C>A) | gnomAD v4 |
7 | g.81729567G>A | CA1720888216 | HGF | c.1040+38C>T (n.1040+38C>T) c.1025+38C>T (n.1025+38C>T) | dbSNP gnomAD v4 |
7 | g.81729567G= | CA1720888215 | HGF | c.1040+38C= (n.1040+38C=) c.1025+38C= (n.1025+38C=) | |
7 | g.81729567G>T | CA2578923862 | HGF | c.1040+38C>A (n.1040+38C>A) c.1025+38C>A (n.1025+38C>A) | gnomAD v4 |
7 | g.81729568C>T | CA2683531192 | HGF | c.1040+37G>A (n.1040+37G>A) c.1025+37G>A (n.1025+37G>A) | dbSNP gnomAD v4 |
7 | g.81729569C>A | CA2683531193 | HGF | c.1040+36G>T (n.1040+36G>T) c.1025+36G>T (n.1025+36G>T) | gnomAD v4 |
7 | g.81729569C>T | CA2578923863 | HGF | c.1040+36G>A (n.1040+36G>A) c.1025+36G>A (n.1025+36G>A) | gnomAD v4 |
7 | g.81729570T>C | CA2683531194 | HGF | c.1040+35A>G (n.1040+35A>G) c.1025+35A>G (n.1025+35A>G) | gnomAD v4 |
7 | g.81729571A= | CA1720888217 | HGF | c.1040+34T= (n.1040+34T=) c.1025+34T= (n.1025+34T=) | |
7 | g.81729571A>G | CA4317001 | HGF | c.1040+34T>C (n.1040+34T>C) c.1025+34T>C (n.1025+34T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729571A>T | CA2683531195 | HGF | c.1040+34T>A (n.1040+34T>A) c.1025+34T>A (n.1025+34T>A) | gnomAD v4 |
7 | g.81729571_81729572delinsAC | CA1720888218 | HGF | c.1040+33_1040+34delinsGT (n.1040+33_1040+34delinsGT) c.1025+33_1025+34delinsGT (n.1025+33_1025+34delinsGT) | |
7 | g.81729572del | CA842849628 | HGF | c.1040+33del (n.1040+33del) c.1025+33del (n.1025+33del) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.81729572C= | CA1720888219 | HGF | c.1040+33G= (n.1040+33G=) c.1025+33G= (n.1025+33G=) | |
7 | g.81729572C>T | CA161089639 | HGF | c.1040+33G>A (n.1040+33G>A) c.1025+33G>A (n.1025+33G>A) | dbSNP gnomAD v4 |
7 | g.81729573T>C | CA4317002 | HGF | c.1040+32A>G (n.1040+32A>G) c.1025+32A>G (n.1025+32A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.81729573T= | CA1720888220 | HGF | c.1040+32A= (n.1040+32A=) c.1025+32A= (n.1025+32A=) | |
7 | g.81729574G>T | CA2683531196 | HGF | c.1040+31C>A (n.1040+31C>A) c.1025+31C>A (n.1025+31C>A) | gnomAD v4 |
7 | g.81729575A= | CA1720888221 | HGF | c.1040+30T= (n.1040+30T=) c.1025+30T= (n.1025+30T=) | |
7 | g.81729575A>T | CA4317003 | HGF | c.1040+30T>A (n.1040+30T>A) c.1025+30T>A (n.1025+30T>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.81729576A= | CA1720888222 | HGF | c.1040+29T= (n.1040+29T=) c.1025+29T= (n.1025+29T=) | |
7 | g.81729576A>C | CA2578923864 | HGF | c.1040+29T>G (n.1040+29T>G) c.1025+29T>G (n.1025+29T>G) | gnomAD v4 |
7 | g.81729576A>G | CA842849633 | HGF | c.1040+29T>C (n.1040+29T>C) c.1025+29T>C (n.1025+29T>C) | dbSNP gnomAD v4 |
7 | g.81729577A>G | CA2683531197 | HGF | c.1040+28T>C (n.1040+28T>C) c.1025+28T>C (n.1025+28T>C) | gnomAD v4 |
7 | g.81729578T>C | CA575808882 | HGF | c.1040+27A>G (n.1040+27A>G) c.1025+27A>G (n.1025+27A>G) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729578T= | CA1720888223 | HGF | c.1040+27A= (n.1040+27A=) c.1025+27A= (n.1025+27A=) | |
7 | g.81729579G>A | CA575808884 | HGF | c.1040+26C>T (n.1040+26C>T) c.1025+26C>T (n.1025+26C>T) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729579G= | CA1720888224 | HGF | c.1040+26C= (n.1040+26C=) c.1025+26C= (n.1025+26C=) | |
7 | g.81729579G>T | CA575808883 | HGF | c.1040+26C>A (n.1040+26C>A) c.1025+26C>A (n.1025+26C>A) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729580T>G | CA2683531198 | HGF | c.1040+25A>C (n.1040+25A>C) c.1025+25A>C (n.1025+25A>C) | gnomAD v4 |
7 | g.81729581A= | CA1720888225 | HGF | c.1040+24T= (n.1040+24T=) c.1025+24T= (n.1025+24T=) | |
7 | g.81729581A>G | CA842849657 | HGF | c.1040+24T>C (n.1040+24T>C) c.1025+24T>C (n.1025+24T>C) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.81729582T>C | CA1720888227 | HGF | c.1040+23A>G (n.1040+23A>G) c.1025+23A>G (n.1025+23A>G) | dbSNP |
7 | g.81729582T= | CA1720888226 | HGF | c.1040+23A= (n.1040+23A=) c.1025+23A= (n.1025+23A=) | |
7 | g.81729583A= | CA1720888228 | HGF | c.1040+22T= (n.1040+22T=) c.1025+22T= (n.1025+22T=) | |
7 | g.81729583A>G | CA575808885 | HGF | c.1040+22T>C (n.1040+22T>C) c.1025+22T>C (n.1025+22T>C) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729584del | CA2683531199 | HGF | c.1040+22del (n.1040+22del) c.1025+22del (n.1025+22del) | gnomAD v4 |
7 | g.81729584A>G | CA2683531200 | HGF | c.1040+21T>C (n.1040+21T>C) c.1025+21T>C (n.1025+21T>C) | gnomAD v4 |
7 | g.81729585C= | CA1720888229 | HGF | c.1040+20G= (n.1040+20G=) c.1025+20G= (n.1025+20G=) | |
7 | g.81729585C>T | CA575808886 | HGF | c.1040+20G>A (n.1040+20G>A) c.1025+20G>A (n.1025+20G>A) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729586A= | CA1720888230 | HGF | c.1040+19T= (n.1040+19T=) c.1025+19T= (n.1025+19T=) | |
7 | g.81729586A>C | CA2578923865 | HGF | c.1040+19T>G (n.1040+19T>G) c.1025+19T>G (n.1025+19T>G) | |
7 | g.81729586A>T | CA161089648 | HGF | c.1040+19T>A (n.1040+19T>A) c.1025+19T>A (n.1025+19T>A) | dbSNP |
7 | g.81729587T>A | CA2683531201 | HGF | c.1040+18A>T (n.1040+18A>T) c.1025+18A>T (n.1025+18A>T) | gnomAD v4 |
7 | g.81729587T>C | CA161089649 | HGF | c.1040+18A>G (n.1040+18A>G) c.1025+18A>G (n.1025+18A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729587T= | CA1720888231 | HGF | c.1040+18A= (n.1040+18A=) c.1025+18A= (n.1025+18A=) | |
7 | g.81729588T>C | CA1103714078 | HGF | c.1040+17A>G (n.1040+17A>G) c.1025+17A>G (n.1025+17A>G) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.81729588T= | CA1720888232 | HGF | c.1040+17A= (n.1040+17A=) c.1025+17A= (n.1025+17A=) | |
7 | g.81729590G>C | CA4317004 | HGF | c.1040+15C>G (n.1040+15C>G) c.1025+15C>G (n.1025+15C>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729590G= | CA1720888233 | HGF | c.1040+15C= (n.1040+15C=) c.1025+15C= (n.1025+15C=) | |
7 | g.81729590G>T | CA2683531202 | HGF | c.1040+15C>A (n.1040+15C>A) c.1025+15C>A (n.1025+15C>A) | gnomAD v4 |
7 | g.81729591C>A | CA2683531203 | HGF | c.1040+14G>T (n.1040+14G>T) c.1025+14G>T (n.1025+14G>T) | gnomAD v4 |
7 | g.81729591C>T | CA2578923866 | HGF | c.1040+14G>A (n.1040+14G>A) c.1025+14G>A (n.1025+14G>A) | gnomAD v4 |
7 | g.81729592C>G | CA2578923867 | HGF | c.1040+13G>C (n.1040+13G>C) c.1025+13G>C (n.1025+13G>C) | |
7 | g.81729594A= | CA1720888234 | HGF | c.1040+11T= (n.1040+11T=) c.1025+11T= (n.1025+11T=) | |
7 | g.81729594A>G | CA4317005 | HGF | c.1040+11T>C (n.1040+11T>C) c.1025+11T>C (n.1025+11T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729595C>A | CA645562751 | HGF | c.1040+10G>T (n.1040+10G>T) c.1025+10G>T (n.1025+10G>T) | COSMIC |
7 | g.81729595C>T | CA2715096619 | HGF | c.1040+10G>A (n.1040+10G>A) c.1025+10G>A (n.1025+10G>A) | dbSNP |
7 | g.81729596T>G | CA161089661 | HGF | c.1040+9A>C (n.1040+9A>C) c.1025+9A>C (n.1025+9A>C) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.81729596T= | CA1720888235 | HGF | c.1040+9A= (n.1040+9A=) c.1025+9A= (n.1025+9A=) | |
7 | g.81729597T>C | CA4317006 | HGF | c.1040+8A>G (n.1040+8A>G) c.1025+8A>G (n.1025+8A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729597T= | CA1720888236 | HGF | c.1040+8A= (n.1040+8A=) c.1025+8A= (n.1025+8A=) | |
7 | g.81729598T>C | CA4317007 | HGF | c.1040+7A>G (n.1040+7A>G) c.1025+7A>G (n.1025+7A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729598T= | CA1720888237 | HGF | c.1040+7A= (n.1040+7A=) c.1025+7A= (n.1025+7A=) | |
7 | g.81729602C= | CA1720888238 | HGF | c.1040+3G= (n.1040+3G=) c.1025+3G= (n.1025+3G=) | |
7 | g.81729602C>G | CA2683531204 | HGF | c.1040+3G>C (n.1040+3G>C) c.1025+3G>C (n.1025+3G>C) | gnomAD v4 |
7 | g.81729602C>T | CA1103714079 | HGF | c.1040+3G>A (n.1040+3G>A) c.1025+3G>A (n.1025+3G>A) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.81729603_81729604del | CA2578923868 | HGF | c.1040+2_1040+3del (n.1040+2_1040+3del) c.1025+2_1025+3del (n.1025+2_1025+3del) | |
7 | g.81729603A>C | CA367870697 | HGF | c.1040+2T>G (n.1040+2T>G) c.1025+2T>G (n.1025+2T>G) | |
7 | g.81729603A>G | CA367870698 | HGF | c.1040+2T>C (n.1040+2T>C) c.1025+2T>C (n.1025+2T>C) | |
7 | g.81729603A>T | CA367870699 | HGF | c.1040+2T>A (n.1040+2T>A) c.1025+2T>A (n.1025+2T>A) | |
7 | g.81729604C>A | CA367870700 | HGF | c.1040+1G>T (n.1040+1G>T) c.1025+1G>T (n.1025+1G>T) | |
7 | g.81729604C>G | CA367870702 | HGF | c.1040+1G>C (n.1040+1G>C) c.1025+1G>C (n.1025+1G>C) | |
7 | g.81729604C>T | CA367870701 | HGF | c.1040+1G>A (n.1040+1G>A) c.1025+1G>A (n.1025+1G>A) | |
7 | g.81729605T>A | CA367870703 | HGF | c.1040A>T (p.Lys347Met) c.1025A>T (p.Lys342Met) | |
7 | g.81729605T>C | CA367870704 | HGF | c.1040A>G (p.Lys347Arg) c.1025A>G (p.Lys342Arg) | gnomAD v4 |
7 | g.81729605T>G | CA367870705 | HGF | c.1040A>C (p.Lys347Thr) c.1025A>C (p.Lys342Thr) | |
7 | g.81729606T>A | CA367870706 | HGF | c.1039A>T (p.Lys347Ter) c.1024A>T (p.Lys342Ter) | |
7 | g.81729606T>C | CA367870707 | HGF | c.1039A>G (p.Lys347Glu) c.1024A>G (p.Lys342Glu) | |
7 | g.81729606T>G | CA367870708 | HGF | c.1039A>C (p.Lys347Gln) c.1024A>C (p.Lys342Gln) | |
7 | g.81729607G>A | CA456129137 | HGF | c.1038C>T (p.Cys346=) c.1023C>T (p.Cys341=) | |
7 | g.81729607G>C | CA367870709 | HGF | c.1038C>G (p.Cys346Trp) c.1023C>G (p.Cys341Trp) | |
7 | g.81729607G>T | CA367870710 | HGF | c.1038C>A (p.Cys346Ter) c.1023C>A (p.Cys341Ter) | gnomAD v4 |
7 | g.81729608C>A | CA367870711 | HGF | c.1037G>T (p.Cys346Phe) c.1022G>T (p.Cys341Phe) | |
7 | g.81729608C= | CA1720888239 | HGF | c.1037G= (p.Cys346=) c.1022G= (p.Cys341=) | |
7 | g.81729608C>G | CA367870712 | HGF | c.1037G>C (p.Cys346Ser) c.1022G>C (p.Cys341Ser) | |
7 | g.81729608C>T | CA4317008 | HGF | c.1037G>A (p.Cys346Tyr) c.1022G>A (p.Cys341Tyr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.81729609A>C | CA367870713 | HGF | c.1036T>G (p.Cys346Gly) c.1021T>G (p.Cys341Gly) | gnomAD v4 |
7 | g.81729609A>G | CA367870715 | HGF | c.1036T>C (p.Cys346Arg) c.1021T>C (p.Cys341Arg) | gnomAD v4 |
7 | g.81729609A>T | CA367870714 | HGF | c.1036T>A (p.Cys346Ser) c.1021T>A (p.Cys341Ser) | |
7 | g.81729610C>A | CA367870716 | HGF | c.1035G>T (p.Lys345Asn) c.1020G>T (p.Lys340Asn) | |
7 | g.81729610C= | CA1720888240 | HGF | c.1035G= (p.Lys345=) c.1020G= (p.Lys340=) | |
7 | g.81729610C>G | CA367870717 | HGF | c.1035G>C (p.Lys345Asn) c.1020G>C (p.Lys340Asn) | |
7 | g.81729610C>T | CA4317009 | HGF | c.1035G>A (p.Lys345=) c.1020G>A (p.Lys340=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729611T>A | CA367870718 | HGF | c.1034A>T (p.Lys345Met) c.1019A>T (p.Lys340Met) | |
7 | g.81729611T>C | CA367870719 | HGF | c.1034A>G (p.Lys345Arg) c.1019A>G (p.Lys340Arg) | gnomAD v4 |
7 | g.81729611T>G | CA367870720 | HGF | c.1034A>C (p.Lys345Thr) c.1019A>C (p.Lys340Thr) | |
7 | g.81729612T>A | CA367870721 | HGF | c.1033A>T (p.Lys345Ter) c.1018A>T (p.Lys340Ter) | |
7 | g.81729612T>C | CA367870722 | HGF | c.1033A>G (p.Lys345Glu) c.1018A>G (p.Lys340Glu) | dbSNP |
7 | g.81729612T>G | CA367870723 | HGF | c.1033A>C (p.Lys345Gln) c.1018A>C (p.Lys340Gln) | gnomAD v4 |
7 | g.81729613G>A | CA456129138 | HGF | c.1032C>T (p.Phe344=) c.1017C>T (p.Phe339=) | COSMIC |
7 | g.81729613G>C | CA367870724 | HGF | c.1032C>G (p.Phe344Leu) c.1017C>G (p.Phe339Leu) | |
7 | g.81729613G>T | CA367870725 | HGF | c.1032C>A (p.Phe344Leu) c.1017C>A (p.Phe339Leu) | |
7 | g.81729614A>C | CA367870728 | HGF | c.1031T>G (p.Phe344Cys) c.1016T>G (p.Phe339Cys) | |
7 | g.81729614A>G | CA367870727 | HGF | c.1031T>C (p.Phe344Ser) c.1016T>C (p.Phe339Ser) | |
7 | g.81729614A>T | CA367870726 | HGF | c.1031T>A (p.Phe344Tyr) c.1016T>A (p.Phe339Tyr) | |
7 | g.81729615A>C | CA367870729 | HGF | c.1030T>G (p.Phe344Val) c.1015T>G (p.Phe339Val) | |
7 | g.81729615A>G | CA367870730 | HGF | c.1030T>C (p.Phe344Leu) c.1015T>C (p.Phe339Leu) | |
7 | g.81729615A>T | CA367870731 | HGF | c.1030T>A (p.Phe344Ile) c.1015T>A (p.Phe339Ile) | |
7 | g.81729616A= | CA1720888241 | HGF | c.1029T= (p.Asn343=) c.1014T= (p.Asn338=) | |
7 | g.81729616A>C | CA367870732 | HGF | c.1029T>G (p.Asn343Lys) c.1014T>G (p.Asn338Lys) | |
7 | g.81729616A>G | CA4317010 | HGF | c.1029T>C (p.Asn343=) c.1014T>C (p.Asn338=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.81729616A>T | CA367870733 | HGF | c.1029T>A (p.Asn343Lys) c.1014T>A (p.Asn338Lys) | |
7 | g.81729617T>A | CA367870734 | HGF | c.1028A>T (p.Asn343Ile) c.1013A>T (p.Asn338Ile) | |
7 | g.81729617T>C | CA367870735 | HGF | c.1028A>G (p.Asn343Ser) c.1013A>G (p.Asn338Ser) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729617T>G | CA367870736 | HGF | c.1028A>C (p.Asn343Thr) c.1013A>C (p.Asn338Thr) | |
7 | g.81729617T= | CA1720888242 | HGF | c.1028A= (p.Asn343=) c.1013A= (p.Asn338=) | |
7 | g.81729618T>A | CA367870737 | HGF | c.1027A>T (p.Asn343Tyr) c.1012A>T (p.Asn338Tyr) | gnomAD v4 |
7 | g.81729618T>C | CA367870738 | HGF | c.1027A>G (p.Asn343Asp) c.1012A>G (p.Asn338Asp) | |
7 | g.81729618T>G | CA367870739 | HGF | c.1027A>C (p.Asn343His) c.1012A>C (p.Asn338His) | |
7 | g.81729619T>A | CA367870741 | HGF | c.1026A>T (p.Glu342Asp) c.1011A>T (p.Glu337Asp) | |
7 | g.81729619T>C | CA456129139 | HGF | c.1026A>G (p.Glu342=) c.1011A>G (p.Glu337=) | |
7 | g.81729619T>G | CA367870740 | HGF | c.1026A>C (p.Glu342Asp) c.1011A>C (p.Glu337Asp) | |
7 | g.81729620T>A | CA367870742 | HGF | c.1025A>T (p.Glu342Val) c.1010A>T (p.Glu337Val) | |
7 | g.81729620T>C | CA367870744 | HGF | c.1025A>G (p.Glu342Gly) c.1010A>G (p.Glu337Gly) | |
7 | g.81729620T>G | CA367870743 | HGF | c.1025A>C (p.Glu342Ala) c.1010A>C (p.Glu337Ala) | |
7 | g.81729621C>A | CA367870745 | HGF | c.1024G>T (p.Glu342Ter) c.1009G>T (p.Glu337Ter) | |
7 | g.81729621C>G | CA367870746 | HGF | c.1024G>C (p.Glu342Gln) c.1009G>C (p.Glu337Gln) | |
7 | g.81729621C>T | CA367870747 | HGF | c.1024G>A (p.Glu342Lys) c.1009G>A (p.Glu337Lys) | COSMIC |
7 | g.81729622A>C | CA456129140 | HGF | c.1023T>G (p.Pro341=) c.1008T>G (p.Pro336=) | |
7 | g.81729622A>G | CA456129141 | HGF | c.1023T>C (p.Pro341=) c.1008T>C (p.Pro336=) | gnomAD v4 |
7 | g.81729622A>T | CA456129142 | HGF | c.1023T>A (p.Pro341=) c.1008T>A (p.Pro336=) | |
7 | g.81729623G>A | CA367870748 | HGF | c.1022C>T (p.Pro341Leu) c.1007C>T (p.Pro336Leu) | |
7 | g.81729623G>C | CA367870749 | HGF | c.1022C>G (p.Pro341Arg) c.1007C>G (p.Pro336Arg) | |
7 | g.81729623G>T | CA367870750 | HGF | c.1022C>A (p.Pro341His) c.1007C>A (p.Pro336His) | |
7 | g.81729624G>A | CA367870751 | HGF | c.1021C>T (p.Pro341Ser) c.1006C>T (p.Pro336Ser) | |
7 | g.81729624G>C | CA367870752 | HGF | c.1021C>G (p.Pro341Ala) c.1006C>G (p.Pro336Ala) | |
7 | g.81729624G>T | CA367870753 | HGF | c.1021C>A (p.Pro341Thr) c.1006C>A (p.Pro336Thr) | |
7 | g.81729625A>C | CA456129143 | HGF | c.1020T>G (p.Thr340=) c.1005T>G (p.Thr335=) | |
7 | g.81729625A>G | CA456129144 | HGF | c.1020T>C (p.Thr340=) c.1005T>C (p.Thr335=) | |
7 | g.81729625A>T | CA456129145 | HGF | c.1020T>A (p.Thr340=) c.1005T>A (p.Thr335=) | |
7 | g.81729626G>A | CA367870754 | HGF | c.1019C>T (p.Thr340Ile) c.1004C>T (p.Thr335Ile) | |
7 | g.81729626G>C | CA367870755 | HGF | c.1019C>G (p.Thr340Ser) c.1004C>G (p.Thr335Ser) | gnomAD v4 |
7 | g.81729626G>T | CA367870756 | HGF | c.1019C>A (p.Thr340Asn) c.1004C>A (p.Thr335Asn) | |
7 | g.81729627T>A | CA367870759 | HGF | c.1018A>T (p.Thr340Ser) c.1003A>T (p.Thr335Ser) | |
7 | g.81729627T>C | CA367870757 | HGF | c.1018A>G (p.Thr340Ala) c.1003A>G (p.Thr335Ala) | |
7 | g.81729627T>G | CA367870758 | HGF | c.1018A>C (p.Thr340Pro) c.1003A>C (p.Thr335Pro) | |
7 | g.81729628C>A | CA367870760 | HGF | c.1017G>T (p.Met339Ile) c.1002G>T (p.Met334Ile) | |
7 | g.81729628C= | CA1720888243 | HGF | c.1017G= (p.Met339=) c.1002G= (p.Met334=) | |
7 | g.81729628C>G | CA367870761 | HGF | c.1017G>C (p.Met339Ile) c.1002G>C (p.Met334Ile) | |
7 | g.81729628C>T | CA367870762 | HGF | c.1017G>A (p.Met339Ile) c.1002G>A (p.Met334Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729629A>C | CA367870763 | HGF | c.1016T>G (p.Met339Arg) c.1001T>G (p.Met334Arg) | |
7 | g.81729629A>G | CA367870764 | HGF | c.1016T>C (p.Met339Thr) c.1001T>C (p.Met334Thr) | gnomAD v4 |
7 | g.81729629A>T | CA367870765 | HGF | c.1016T>A (p.Met339Lys) c.1001T>A (p.Met334Lys) | |
7 | g.81729630T>A | CA367870766 | HGF | c.1015A>T (p.Met339Leu) c.1000A>T (p.Met334Leu) | |
7 | g.81729630T>C | CA367870767 | HGF | c.1015A>G (p.Met339Val) c.1000A>G (p.Met334Val) | gnomAD v4 |
7 | g.81729630T>G | CA367870768 | HGF | c.1015A>C (p.Met339Leu) c.1000A>C (p.Met334Leu) | |
7 | g.81729631G>A | CA456129146 | HGF | c.1014C>T (p.Asp338=) c.999C>T (p.Asp333=) | gnomAD v4 |
7 | g.81729631G>C | CA367870769 | HGF | c.1014C>G (p.Asp338Glu) c.999C>G (p.Asp333Glu) | |
7 | g.81729631G>T | CA367870770 | HGF | c.1014C>A (p.Asp338Glu) c.999C>A (p.Asp333Glu) | ClinVar |
7 | g.81729632T>A | CA367870773 | HGF | c.1013A>T (p.Asp338Val) c.998A>T (p.Asp333Val) | |
7 | g.81729632T>C | CA367870772 | HGF | c.1013A>G (p.Asp338Gly) c.998A>G (p.Asp333Gly) | |
7 | g.81729632T>G | CA367870771 | HGF | c.1013A>C (p.Asp338Ala) c.998A>C (p.Asp333Ala) | |
7 | g.81729633C>A | CA367870774 | HGF | c.1012G>T (p.Asp338Tyr) c.997G>T (p.Asp333Tyr) | |
7 | g.81729633C>G | CA367870775 | HGF | c.1012G>C (p.Asp338His) c.997G>C (p.Asp333His) | |
7 | g.81729633C>T | CA367870776 | HGF | c.1012G>A (p.Asp338Asn) c.997G>A (p.Asp333Asn) | dbSNP |
7 | g.81729634A= | CA1720888244 | HGF | c.1011T= (p.His337=) c.996T= (p.His332=) | |
7 | g.81729634A>C | CA367870777 | HGF | c.1011T>G (p.His337Gln) c.996T>G (p.His332Gln) | |
7 | g.81729634A>G | CA456129147 | HGF | c.1011T>C (p.His337=) c.996T>C (p.His332=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729634A>T | CA367870778 | HGF | c.1011T>A (p.His337Gln) c.996T>A (p.His332Gln) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729635T>A | CA367870781 | HGF | c.1010A>T (p.His337Leu) c.995A>T (p.His332Leu) | |
7 | g.81729635T>C | CA367870780 | HGF | c.1010A>G (p.His337Arg) c.995A>G (p.His332Arg) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729635T>G | CA367870779 | HGF | c.1010A>C (p.His337Pro) c.995A>C (p.His332Pro) | |
7 | g.81729635T= | CA1720888245 | HGF | c.1010A= (p.His337=) c.995A= (p.His332=) | |
7 | g.81729636G>A | CA367870782 | HGF | c.1009C>T (p.His337Tyr) c.994C>T (p.His332Tyr) | |
7 | g.81729636G>C | CA367870783 | HGF | c.1009C>G (p.His337Asp) c.994C>G (p.His332Asp) | |
7 | g.81729636G>T | CA367870784 | HGF | c.1009C>A (p.His337Asn) c.994C>A (p.His332Asn) | gnomAD v4 |
7 | g.81729637C>A | CA367870785 | HGF | c.1008G>T (p.Glu336Asp) c.993G>T (p.Glu331Asp) | |
7 | g.81729637C= | CA1720888246 | HGF | c.1008G= (p.Glu336=) c.993G= (p.Glu331=) | |
7 | g.81729637C>G | CA367870786 | HGF | c.1008G>C (p.Glu336Asp) c.993G>C (p.Glu331Asp) | |
7 | g.81729637C>T | CA132813 | HGF | c.1008G>A (p.Glu336=) c.993G>A (p.Glu331=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729638T>A | CA367870787 | HGF | c.1007A>T (p.Glu336Val) c.992A>T (p.Glu331Val) | |
7 | g.81729638T>C | CA367870789 | HGF | c.1007A>G (p.Glu336Gly) c.992A>G (p.Glu331Gly) | |
7 | g.81729638T>G | CA367870788 | HGF | c.1007A>C (p.Glu336Ala) c.992A>C (p.Glu331Ala) | |
7 | g.81729639C>A | CA367870790 | HGF | c.1006G>T (p.Glu336Ter) c.991G>T (p.Glu331Ter) | |
7 | g.81729639C= | CA1720888247 | HGF | c.1006G= (p.Glu336=) c.991G= (p.Glu331=) | |
7 | g.81729639C>G | CA367870791 | HGF | c.1006G>C (p.Glu336Gln) c.991G>C (p.Glu331Gln) | |
7 | g.81729639C>T | CA4317011 | HGF | c.1006G>A (p.Glu336Lys) c.991G>A (p.Glu331Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729640G>A | CA4317012 | HGF | c.1005C>T (p.His335=) c.990C>T (p.His330=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729640G>C | CA367870792 | HGF | c.1005C>G (p.His335Gln) c.990C>G (p.His330Gln) | |
7 | g.81729640G= | CA1720888248 | HGF | c.1005C= (p.His335=) c.990C= (p.His330=) | |
7 | g.81729640G>T | CA367870793 | HGF | c.1005C>A (p.His335Gln) c.990C>A (p.His330Gln) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729641T>A | CA367870794 | HGF | c.1004A>T (p.His335Leu) c.989A>T (p.His330Leu) | |
7 | g.81729641T>C | CA367870795 | HGF | c.1004A>G (p.His335Arg) c.989A>G (p.His330Arg) | |
7 | g.81729641T>G | CA367870796 | HGF | c.1004A>C (p.His335Pro) c.989A>C (p.His330Pro) | |
7 | g.81729642G>A | CA367870797 | HGF | c.1003C>T (p.His335Tyr) c.988C>T (p.His330Tyr) | dbSNP |
7 | g.81729642G>C | CA367870798 | HGF | c.1003C>G (p.His335Asp) c.988C>G (p.His330Asp) | |
7 | g.81729642G= | CA1720888249 | HGF | c.1003C= (p.His335=) c.988C= (p.His330=) | |
7 | g.81729642G>T | CA367870799 | HGF | c.1003C>A (p.His335Asn) c.988C>A (p.His330Asn) | |
7 | g.81729643A>C | CA456129148 | HGF | c.1002T>G (p.Pro334=) c.987T>G (p.Pro329=) | |
7 | g.81729643A>G | CA456129150 | HGF | c.1002T>C (p.Pro334=) c.987T>C (p.Pro329=) | |
7 | g.81729643A>T | CA456129149 | HGF | c.1002T>A (p.Pro334=) c.987T>A (p.Pro329=) | |
7 | g.81729644G>A | CA367870801 | HGF | c.1001C>T (p.Pro334Leu) c.986C>T (p.Pro329Leu) | dbSNP |
7 | g.81729644G>C | CA367870802 | HGF | c.1001C>G (p.Pro334Arg) c.986C>G (p.Pro329Arg) | |
7 | g.81729644G>T | CA367870800 | HGF | c.1001C>A (p.Pro334His) c.986C>A (p.Pro329His) | |
7 | g.81729645G>A | CA367870805 | HGF | c.1000C>T (p.Pro334Ser) c.985C>T (p.Pro329Ser) | dbSNP |
7 | g.81729645G>C | CA367870803 | HGF | c.1000C>G (p.Pro334Ala) c.985C>G (p.Pro329Ala) | |
7 | g.81729645G= | CA1720888250 | HGF | c.1000C= (p.Pro334=) c.985C= (p.Pro329=) | |
7 | g.81729645G>T | CA367870804 | HGF | c.1000C>A (p.Pro334Thr) c.985C>A (p.Pro329Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729646A= | CA1720888251 | HGF | c.999T= (p.Tyr333=) c.984T= (p.Tyr328=) | |
7 | g.81729646A>C | CA367870806 | HGF | c.999T>G (p.Tyr333Ter) c.984T>G (p.Tyr328Ter) | |
7 | g.81729646A>G | CA4317013 | HGF | c.999T>C (p.Tyr333=) c.984T>C (p.Tyr328=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729646A>T | CA367870807 | HGF | c.999T>A (p.Tyr333Ter) c.984T>A (p.Tyr328Ter) | |
7 | g.81729647T>A | CA367870808 | HGF | c.998A>T (p.Tyr333Phe) c.983A>T (p.Tyr328Phe) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.81729647T>C | CA367870809 | HGF | c.998A>G (p.Tyr333Cys) c.983A>G (p.Tyr328Cys) | dbSNP |
7 | g.81729647T>G | CA367870810 | HGF | c.998A>C (p.Tyr333Ser) c.983A>C (p.Tyr328Ser) | |
7 | g.81729647T= | CA1720888252 | HGF | c.998A= (p.Tyr333=) c.983A= (p.Tyr328=) | |
7 | g.81729648A>C | CA367870811 | HGF | c.997T>G (p.Tyr333Asp) c.982T>G (p.Tyr328Asp) | |
7 | g.81729648A>G | CA367870812 | HGF | c.997T>C (p.Tyr333His) c.982T>C (p.Tyr328His) | COSMIC |
7 | g.81729648A>T | CA367870813 | HGF | c.997T>A (p.Tyr333Asn) c.982T>A (p.Tyr328Asn) | |
7 | g.81729649C>A | CA367870814 | HGF | c.996G>T (p.Gln332His) c.981G>T (p.Gln327His) | |
7 | g.81729649C= | CA1720888253 | HGF | c.996G= (p.Gln332=) c.981G= (p.Gln327=) | |
7 | g.81729649C>G | CA367870815 | HGF | c.996G>C (p.Gln332His) c.981G>C (p.Gln327His) | |
7 | g.81729649C>T | CA161089691 | HGF | c.996G>A (p.Gln332=) c.981G>A (p.Gln327=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |