Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154928653del | CA2695237906 | F8 | c.5140del (p.Thr1714HisfsTer17) c.5035del (p.Thr1679HisfsTer17) | |
X | g.154928654_154928658del | CA2695237904 | F8 | c.5136_5140del (p.Lys1712AsnfsTer19) c.5031_5035del (p.Lys1677AsnfsTer19) | |
X | g.154928651T>A | CA414913764 | F8 | c.5139A>T (p.Lys1713Asn) c.5034A>T (p.Lys1678Asn) | |
X | g.154928651T>C | CA519718373 | F8 | c.5139A>G (p.Lys1713=) c.5034A>G (p.Lys1678=) | |
X | g.154928651T>G | CA414913766 | F8 | c.5139A>C (p.Lys1713Asn) c.5034A>C (p.Lys1678Asn) | |
X | g.154928652T>A | CA414913769 | F8 | c.5138A>T (p.Lys1713Ile) c.5033A>T (p.Lys1678Ile) | |
X | g.154928652T>C | CA414913773 | F8 | c.5138A>G (p.Lys1713Arg) c.5033A>G (p.Lys1678Arg) | |
X | g.154928652T>G | CA414913771 | F8 | c.5138A>C (p.Lys1713Thr) c.5033A>C (p.Lys1678Thr) | |
X | g.154928653T>A | CA414913779 | F8 | c.5137A>T (p.Lys1713Ter) c.5032A>T (p.Lys1678Ter) | |
X | g.154928653T>C | CA414913781 | F8 | c.5137A>G (p.Lys1713Glu) c.5032A>G (p.Lys1678Glu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154928653T>G | CA414913783 | F8 | c.5137A>C (p.Lys1713Gln) c.5032A>C (p.Lys1678Gln) | |
X | g.154928653T= | CA2466835756 | F8 | c.5137A= (p.Lys1713=) c.5032A= (p.Lys1678=) | |
X | g.154928654C>A | CA414913785 | F8 | c.5136G>T (p.Lys1712Asn) c.5031G>T (p.Lys1677Asn) | dbSNP COSMIC COSMIC |
X | g.154928654C= | CA2466835757 | F8 | c.5136G= (p.Lys1712=) c.5031G= (p.Lys1677=) | |
X | g.154928654C>G | CA414913786 | F8 | c.5136G>C (p.Lys1712Asn) c.5031G>C (p.Lys1677Asn) | ClinVar dbSNP gnomAD v4 |
X | g.154928654C>T | CA10568035 | F8 | c.5136G>A (p.Lys1712=) c.5031G>A (p.Lys1677=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154928655T>A | CA414913789 | F8 | c.5135A>T (p.Lys1712Met) c.5030A>T (p.Lys1677Met) | |
X | g.154928655T>C | CA414913791 | F8 | c.5135A>G (p.Lys1712Arg) c.5030A>G (p.Lys1677Arg) | gnomAD v4 |
X | g.154928655T>G | CA414913793 | F8 | c.5135A>C (p.Lys1712Thr) c.5030A>C (p.Lys1677Thr) | |
X | g.154928656T>A | CA414913797 | F8 | c.5134A>T (p.Lys1712Ter) c.5029A>T (p.Lys1677Ter) | |
X | g.154928656T>C | CA414913799 | F8 | c.5134A>G (p.Lys1712Glu) c.5029A>G (p.Lys1677Glu) | |
X | g.154928656T>G | CA414913795 | F8 | c.5134A>C (p.Lys1712Gln) c.5029A>C (p.Lys1677Gln) | |
X | g.154928657T>A | CA414913801 | F8 | c.5133A>T (p.Gln1711His) c.5028A>T (p.Gln1676His) | |
X | g.154928657T>C | CA519718374 | F8 | c.5133A>G (p.Gln1711=) c.5028A>G (p.Gln1676=) | |
X | g.154928657T>G | CA414913802 | F8 | c.5133A>C (p.Gln1711His) c.5028A>C (p.Gln1676His) | |
X | g.154928658T>A | CA414913804 | F8 | c.5132A>T (p.Gln1711Leu) c.5027A>T (p.Gln1676Leu) | |
X | g.154928658T>C | CA414913806 | F8 | c.5132A>G (p.Gln1711Arg) c.5027A>G (p.Gln1676Arg) | |
X | g.154928658T>G | CA414913807 | F8 | c.5132A>C (p.Gln1711Pro) c.5027A>C (p.Gln1676Pro) | ClinVar |
X | g.154928659G>A | CA414913813 | F8 | c.5131C>T (p.Gln1711Ter) c.5026C>T (p.Gln1676Ter) | |
X | g.154928659G>C | CA414913810 | F8 | c.5131C>G (p.Gln1711Glu) c.5026C>G (p.Gln1676Glu) | COSMIC COSMIC |
X | g.154928659G= | CA2466835758 | F8 | c.5131C= (p.Gln1711=) c.5026C= (p.Gln1676=) | |
X | g.154928659G>T | CA414913812 | F8 | c.5131C>A (p.Gln1711Lys) c.5026C>A (p.Gln1676Lys) | dbSNP gnomAD v4 |
X | g.154928660A>C | CA414913815 | F8 | c.5130T>G (p.Phe1710Leu) c.5025T>G (p.Phe1675Leu) | |
X | g.154928660A>G | CA519718375 | F8 | c.5130T>C (p.Phe1710=) c.5025T>C (p.Phe1675=) | |
X | g.154928660A>T | CA414913816 | F8 | c.5130T>A (p.Phe1710Leu) c.5025T>A (p.Phe1675Leu) | dbSNP gnomAD v4 |
X | g.154928662del | CA2695237912 | F8 | c.5130del (p.Gln1711LysfsTer20) c.5025del (p.Gln1676LysfsTer20) | |
X | g.154928661A>C | CA414913818 | F8 | c.5129T>G (p.Phe1710Cys) c.5024T>G (p.Phe1675Cys) | |
X | g.154928661A>G | CA414913819 | F8 | c.5129T>C (p.Phe1710Ser) c.5024T>C (p.Phe1675Ser) | |
X | g.154928661A>T | CA414913821 | F8 | c.5129T>A (p.Phe1710Tyr) c.5024T>A (p.Phe1675Tyr) | |
X | g.154928662A>C | CA414913823 | F8 | c.5128T>G (p.Phe1710Val) c.5023T>G (p.Phe1675Val) | |
X | g.154928662A>G | CA414913827 | F8 | c.5128T>C (p.Phe1710Leu) c.5023T>C (p.Phe1675Leu) | |
X | g.154928662A>T | CA414913825 | F8 | c.5128T>A (p.Phe1710Ile) c.5023T>A (p.Phe1675Ile) | |
X | g.154928663G>A | CA519718376 | F8 | c.5127C>T (p.Ser1709=) c.5022C>T (p.Ser1674=) | gnomAD v4 |
X | g.154928663G>C | CA414913829 | F8 | c.5127C>G (p.Ser1709Arg) c.5022C>G (p.Ser1674Arg) | dbSNP |
X | g.154928663G>T | CA414913831 | F8 | c.5127C>A (p.Ser1709Arg) c.5022C>A (p.Ser1674Arg) | |
X | g.154928664C>A | CA414913833 | F8 | c.5126G>T (p.Ser1709Ile) c.5021G>T (p.Ser1674Ile) | |
X | g.154928664C= | CA2466835759 | F8 | c.5126G= (p.Ser1709=) c.5021G= (p.Ser1674=) | |
X | g.154928664C>G | CA414913835 | F8 | c.5126G>C (p.Ser1709Thr) c.5021G>C (p.Ser1674Thr) | |
X | g.154928664C>T | CA414913836 | F8 | c.5126G>A (p.Ser1709Asn) c.5021G>A (p.Ser1674Asn) | dbSNP |
X | g.154928665del | CA2695237914 | F8 | c.5125del (p.Ser1709AlafsTer22) c.5020del (p.Ser1674AlafsTer22) | |
X | g.154928665T>A | CA414913838 | F8 | c.5125A>T (p.Ser1709Cys) c.5020A>T (p.Ser1674Cys) | |
X | g.154928665T>C | CA414913839 | F8 | c.5125A>G (p.Ser1709Gly) c.5020A>G (p.Ser1674Gly) | |
X | g.154928665T>G | CA414913840 | F8 | c.5125A>C (p.Ser1709Arg) c.5020A>C (p.Ser1674Arg) | |
X | g.154928666G>A | CA519718377 | F8 | c.5124C>T (p.Arg1708=) c.5019C>T (p.Arg1673=) | |
X | g.154928666G>C | CA519718378 | F8 | c.5124C>G (p.Arg1708=) c.5019C>G (p.Arg1673=) | |
X | g.154928666G>T | CA519718379 | F8 | c.5124C>A (p.Arg1708=) c.5019C>A (p.Arg1673=) | |
X | g.154928667C>A | CA414913841 | F8 | c.5123G>T (p.Arg1708Leu) c.5018G>T (p.Arg1673Leu) | |
X | g.154928667C= | CA2466835760 | F8 | c.5123G= (p.Arg1708=) c.5018G= (p.Arg1673=) | |
X | g.154928667C>G | CA414913842 | F8 | c.5123G>C (p.Arg1708Pro) c.5018G>C (p.Arg1673Pro) | |
X | g.154928667C>T | CA255154 | F8 | c.5123G>A (p.Arg1708His) c.5018G>A (p.Arg1673His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
X | g.154928667_154928668delinsCG | CA2466835761 | F8 | c.5122_5123delinsCG (p.Arg1708=) c.5017_5018delinsCG (p.Arg1673=) | |
X | g.154928668G>A | CA120919 | F8 | c.5122C>T (p.Arg1708Cys) c.5017C>T (p.Arg1673Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
X | g.154928668G>C | CA414913845 | F8 | c.5122C>G (p.Arg1708Gly) c.5017C>G (p.Arg1673Gly) | |
X | g.154928668G= | CA2466835762 | F8 | c.5122C= (p.Arg1708=) c.5017C= (p.Arg1673=) | |
X | g.154928668G>T | CA414913844 | F8 | c.5122C>A (p.Arg1708Ser) c.5017C>A (p.Arg1673Ser) | dbSNP |
X | g.154928672dup | CA2824302241 | F8 | c.5122dup (p.Arg1708ProfsTer25) c.5017dup (p.Arg1673ProfsTer25) | |
X | g.154928672del | CA873340216 | F8 | c.5122del (p.Arg1708AlafsTer23) c.5017del (p.Arg1673AlafsTer23) | dbSNP |
X | g.154928669G>A | CA519718380 | F8 | c.5121C>T (p.Pro1707=) c.5016C>T (p.Pro1672=) | |
X | g.154928669G>C | CA519718381 | F8 | c.5121C>G (p.Pro1707=) c.5016C>G (p.Pro1672=) | |
X | g.154928669G>T | CA519718382 | F8 | c.5121C>A (p.Pro1707=) c.5016C>A (p.Pro1672=) | gnomAD v4 |
X | g.154928670G>A | CA10568036 | F8 | c.5120C>T (p.Pro1707Leu) c.5015C>T (p.Pro1672Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154928670G>C | CA414913848 | F8 | c.5120C>G (p.Pro1707Arg) c.5015C>G (p.Pro1672Arg) | |
X | g.154928670G= | CA2466835763 | F8 | c.5120C= (p.Pro1707=) c.5015C= (p.Pro1672=) | |
X | g.154928670G>T | CA414913847 | F8 | c.5120C>A (p.Pro1707His) c.5015C>A (p.Pro1672His) | |
X | g.154928671G>A | CA414913850 | F8 | c.5119C>T (p.Pro1707Ser) c.5014C>T (p.Pro1672Ser) | |
X | g.154928671G>C | CA414913853 | F8 | c.5119C>G (p.Pro1707Ala) c.5014C>G (p.Pro1672Ala) | |
X | g.154928671G>T | CA414913851 | F8 | c.5119C>A (p.Pro1707Thr) c.5014C>A (p.Pro1672Thr) | |
X | g.154928672G>A | CA519718383 | F8 | c.5118C>T (p.Ser1706=) c.5013C>T (p.Ser1671=) | gnomAD v4 |
X | g.154928672G>C | CA414913854 | F8 | c.5118C>G (p.Ser1706Arg) c.5013C>G (p.Ser1671Arg) | |
X | g.154928672G>T | CA414913856 | F8 | c.5118C>A (p.Ser1706Arg) c.5013C>A (p.Ser1671Arg) | gnomAD v4 |
X | g.154928673C>A | CA10568037 | F8 | c.5117G>T (p.Ser1706Ile) c.5012G>T (p.Ser1671Ile) | dbSNP ExAC |
X | g.154928673C= | CA2466835764 | F8 | c.5117G= (p.Ser1706=) c.5012G= (p.Ser1671=) | |
X | g.154928673C>G | CA414913858 | F8 | c.5117G>C (p.Ser1706Thr) c.5012G>C (p.Ser1671Thr) | |
X | g.154928673C>T | CA414913860 | F8 | c.5117G>A (p.Ser1706Asn) c.5012G>A (p.Ser1671Asn) | gnomAD v4 |
X | g.154928674T>A | CA414913862 | F8 | c.5116A>T (p.Ser1706Cys) c.5011A>T (p.Ser1671Cys) | |
X | g.154928674T>C | CA414913864 | F8 | c.5116A>G (p.Ser1706Gly) c.5011A>G (p.Ser1671Gly) | |
X | g.154928674T>G | CA414913865 | F8 | c.5116A>C (p.Ser1706Arg) c.5011A>C (p.Ser1671Arg) | |
X | g.154928675C>A | CA414913867 | F8 | c.5115G>T (p.Gln1705His) c.5010G>T (p.Gln1670His) | |
X | g.154928675C>G | CA414913869 | F8 | c.5115G>C (p.Gln1705His) c.5010G>C (p.Gln1670His) | |
X | g.154928675C>T | CA519718384 | F8 | c.5115G>A (p.Gln1705=) c.5010G>A (p.Gln1670=) | |
X | g.154928676del | CA2695237918 | F8 | c.5114del (p.Gln1705ArgfsTer26) c.5009del (p.Gln1670ArgfsTer26) | |
X | g.154928676T>A | CA414913874 | F8 | c.5114A>T (p.Gln1705Leu) c.5009A>T (p.Gln1670Leu) | |
X | g.154928676T>C | CA414913872 | F8 | c.5114A>G (p.Gln1705Arg) c.5009A>G (p.Gln1670Arg) | |
X | g.154928676T>G | CA414913871 | F8 | c.5114A>C (p.Gln1705Pro) c.5009A>C (p.Gln1670Pro) | |
X | g.154928677G>A | CA255020 | F8 | c.5113C>T (p.Gln1705Ter) c.5008C>T (p.Gln1670Ter) | ClinVar dbSNP |
X | g.154928677G>C | CA414913877 | F8 | c.5113C>G (p.Gln1705Glu) c.5008C>G (p.Gln1670Glu) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154928677G= | CA2466835765 | F8 | c.5113C= (p.Gln1705=) c.5008C= (p.Gln1670=) | |
X | g.154928677G>T | CA414913878 | F8 | c.5113C>A (p.Gln1705Lys) c.5008C>A (p.Gln1670Lys) | |
X | g.154928677_154928678dup | CA2695237921 | F8 | c.5112_5113dup (p.Gln1705LeufsTer27) c.5007_5008dup (p.Gln1670LeufsTer27) | |
X | g.154928678A= | CA2466835766 | F8 | c.5112T= (p.Asn1704=) c.5007T= (p.Asn1669=) | |
X | g.154928678A>C | CA414913880 | F8 | c.5112T>G (p.Asn1704Lys) c.5007T>G (p.Asn1669Lys) | gnomAD v4 |
X | g.154928678A>G | CA519718385 | F8 | c.5112T>C (p.Asn1704=) c.5007T>C (p.Asn1669=) | |
X | g.154928678A>T | CA414913882 | F8 | c.5112T>A (p.Asn1704Lys) c.5007T>A (p.Asn1669Lys) | |
X | g.154928679T>A | CA414913884 | F8 | c.5111A>T (p.Asn1704Ile) c.5006A>T (p.Asn1669Ile) | |
X | g.154928679T>C | CA414913886 | F8 | c.5111A>G (p.Asn1704Ser) c.5006A>G (p.Asn1669Ser) | |
X | g.154928679T>G | CA414913887 | F8 | c.5111A>C (p.Asn1704Thr) c.5006A>C (p.Asn1669Thr) | |
X | g.154928681_154928682dup | CA873340243 | F8 | c.5110_5111dup (p.Asn1704LysfsTer28) c.5005_5006dup (p.Asn1669LysfsTer28) | dbSNP |
X | g.154928682del | CA2695237923 | F8 | c.5111del (p.Asn1704IlefsTer27) c.5006del (p.Asn1669IlefsTer27) | |
X | g.154928680T>A | CA414913889 | F8 | c.5110A>T (p.Asn1704Tyr) c.5005A>T (p.Asn1669Tyr) | |
X | g.154928680T>C | CA414913891 | F8 | c.5110A>G (p.Asn1704Asp) c.5005A>G (p.Asn1669Asp) | |
X | g.154928680T>G | CA414913893 | F8 | c.5110A>C (p.Asn1704His) c.5005A>C (p.Asn1669His) | |
X | g.154928681T>A | CA414913895 | F8 | c.5109A>T (p.Glu1703Asp) c.5004A>T (p.Glu1668Asp) | |
X | g.154928681T>C | CA519718386 | F8 | c.5109A>G (p.Glu1703=) c.5004A>G (p.Glu1668=) | |
X | g.154928681T>G | CA414913897 | F8 | c.5109A>C (p.Glu1703Asp) c.5004A>C (p.Glu1668Asp) | |
X | g.154928682T>A | CA414913898 | F8 | c.5108A>T (p.Glu1703Val) c.5003A>T (p.Glu1668Val) | |
X | g.154928682T>C | CA414913899 | F8 | c.5108A>G (p.Glu1703Gly) c.5003A>G (p.Glu1668Gly) | COSMIC COSMIC |
X | g.154928682T>G | CA10568038 | F8 | c.5108A>C (p.Glu1703Ala) c.5003A>C (p.Glu1668Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
X | g.154928682T= | CA2466835767 | F8 | c.5108A= (p.Glu1703=) c.5003A= (p.Glu1668=) | |
X | g.154928683C>A | CA414913902 | F8 | c.5107G>T (p.Glu1703Ter) c.5002G>T (p.Glu1668Ter) | |
X | g.154928683C= | CA2466835768 | F8 | c.5107G= (p.Glu1703=) c.5002G= (p.Glu1668=) | |
X | g.154928683C>G | CA414913903 | F8 | c.5107G>C (p.Glu1703Gln) c.5002G>C (p.Glu1668Gln) | |
X | g.154928683C>T | CA10568039 | F8 | c.5107G>A (p.Glu1703Lys) c.5002G>A (p.Glu1668Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154928684A>C | CA414913905 | F8 | c.5106T>G (p.Asp1702Glu) c.5001T>G (p.Asp1667Glu) | gnomAD v4 |
X | g.154928684A>G | CA519718387 | F8 | c.5106T>C (p.Asp1702=) c.5001T>C (p.Asp1667=) | |
X | g.154928684A>T | CA414913907 | F8 | c.5106T>A (p.Asp1702Glu) c.5001T>A (p.Asp1667Glu) | |
X | g.154928685T>A | CA414913909 | F8 | c.5105A>T (p.Asp1702Val) c.5000A>T (p.Asp1667Val) | |
X | g.154928685T>C | CA414913911 | F8 | c.5105A>G (p.Asp1702Gly) c.5000A>G (p.Asp1667Gly) | |
X | g.154928685T>G | CA414913913 | F8 | c.5105A>C (p.Asp1702Ala) c.5000A>C (p.Asp1667Ala) | |
X | g.154928686C>A | CA414913919 | F8 | c.5104G>T (p.Asp1702Tyr) c.4999G>T (p.Asp1667Tyr) | |
X | g.154928686C>G | CA414913915 | F8 | c.5104G>C (p.Asp1702His) c.4999G>C (p.Asp1667His) | |
X | g.154928686C>T | CA414913917 | F8 | c.5104G>A (p.Asp1702Asn) c.4999G>A (p.Asp1667Asn) | gnomAD v4 COSMIC COSMIC |
X | g.154928687C>A | CA414913921 | F8 | c.5103G>T (p.Glu1701Asp) c.4998G>T (p.Glu1666Asp) | |
X | g.154928687C>G | CA414913923 | F8 | c.5103G>C (p.Glu1701Asp) c.4998G>C (p.Glu1666Asp) | |
X | g.154928687C>T | CA519718388 | F8 | c.5103G>A (p.Glu1701=) c.4998G>A (p.Glu1666=) | |
X | g.154928688T>A | CA414913926 | F8 | c.5102A>T (p.Glu1701Val) c.4997A>T (p.Glu1666Val) | |
X | g.154928688T>C | CA414913928 | F8 | c.5102A>G (p.Glu1701Gly) c.4997A>G (p.Glu1666Gly) | |
X | g.154928688T>G | CA414913929 | F8 | c.5102A>C (p.Glu1701Ala) c.4997A>C (p.Glu1666Ala) | |
X | g.154928689C>A | CA414913931 | F8 | c.5101G>T (p.Glu1701Ter) c.4996G>T (p.Glu1666Ter) | dbSNP |
X | g.154928689C= | CA2466835769 | F8 | c.5101G= (p.Glu1701=) c.4996G= (p.Glu1666=) | |
X | g.154928689C>G | CA414913933 | F8 | c.5101G>C (p.Glu1701Gln) c.4996G>C (p.Glu1666Gln) | |
X | g.154928689C>T | CA414913935 | F8 | c.5101G>A (p.Glu1701Lys) c.4996G>A (p.Glu1666Lys) | ClinVar dbSNP gnomAD v4 |
X | g.154928690A>C | CA414913937 | F8 | c.5100T>G (p.Asp1700Glu) c.4995T>G (p.Asp1665Glu) | |
X | g.154928690A>G | CA519718389 | F8 | c.5100T>C (p.Asp1700=) c.4995T>C (p.Asp1665=) | |
X | g.154928690A>T | CA414913938 | F8 | c.5100T>A (p.Asp1700Glu) c.4995T>A (p.Asp1665Glu) | |
X | g.154928691T>A | CA414913944 | F8 | c.5099A>T (p.Asp1700Val) c.4994A>T (p.Asp1665Val) | |
X | g.154928691T>C | CA414913942 | F8 | c.5099A>G (p.Asp1700Gly) c.4994A>G (p.Asp1665Gly) | gnomAD v4 |
X | g.154928691T>G | CA414913940 | F8 | c.5099A>C (p.Asp1700Ala) c.4994A>C (p.Asp1665Ala) | |
X | g.154928692C>A | CA414913947 | F8 | c.5098G>T (p.Asp1700Tyr) c.4993G>T (p.Asp1665Tyr) | |
X | g.154928692C>G | CA414913949 | F8 | c.5098G>C (p.Asp1700His) c.4993G>C (p.Asp1665His) | |
X | g.154928692C>T | CA414913951 | F8 | c.5098G>A (p.Asp1700Asn) c.4993G>A (p.Asp1665Asn) | |
X | g.154928693A= | CA2466835770 | F8 | c.5097T= (p.Tyr1699=) c.4992T= (p.Tyr1664=) | |
X | g.154928693A>C | CA414913953 | F8 | c.5097T>G (p.Tyr1699Ter) c.4992T>G (p.Tyr1664Ter) | |
X | g.154928693A>G | CA519718390 | F8 | c.5097T>C (p.Tyr1699=) c.4992T>C (p.Tyr1664=) | dbSNP gnomAD v3 gnomAD v4 |
X | g.154928693A>T | CA414913954 | F8 | c.5097T>A (p.Tyr1699Ter) c.4992T>A (p.Tyr1664Ter) | |
X | g.154928694T>A | CA255022 | F8 | c.5096A>T (p.Tyr1699Phe) c.4991A>T (p.Tyr1664Phe) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
X | g.154928694T>C | CA414913958 | F8 | c.5096A>G (p.Tyr1699Cys) c.4991A>G (p.Tyr1664Cys) | dbSNP |
X | g.154928694T>G | CA414913959 | F8 | c.5096A>C (p.Tyr1699Ser) c.4991A>C (p.Tyr1664Ser) | ClinVar dbSNP |
X | g.154928694T= | CA2466835771 | F8 | c.5096A= (p.Tyr1699=) c.4991A= (p.Tyr1664=) | |
X | g.154928695A>C | CA414913961 | F8 | c.5095T>G (p.Tyr1699Asp) c.4990T>G (p.Tyr1664Asp) | |
X | g.154928695A>G | CA414913963 | F8 | c.5095T>C (p.Tyr1699His) c.4990T>C (p.Tyr1664His) | |
X | g.154928695A>T | CA414913964 | F8 | c.5095T>A (p.Tyr1699Asn) c.4990T>A (p.Tyr1664Asn) | COSMIC COSMIC |
X | g.154928696A>C | CA414913967 | F8 | c.5094T>G (p.Ile1698Met) c.4989T>G (p.Ile1663Met) | |
X | g.154928696A>G | CA519718392 | F8 | c.5094T>C (p.Ile1698=) c.4989T>C (p.Ile1663=) | gnomAD v4 |
X | g.154928696A>T | CA519718391 | F8 | c.5094T>A (p.Ile1698=) c.4989T>A (p.Ile1663=) | |
X | g.154928697A= | CA2466835772 | F8 | c.5093T= (p.Ile1698=) c.4988T= (p.Ile1663=) | |
X | g.154928697A>C | CA414913973 | F8 | c.5093T>G (p.Ile1698Ser) c.4988T>G (p.Ile1663Ser) | |
X | g.154928697A>G | CA414913972 | F8 | c.5093T>C (p.Ile1698Thr) c.4988T>C (p.Ile1663Thr) | ClinVar dbSNP gnomAD v4 |
X | g.154928697A>T | CA414913970 | F8 | c.5093T>A (p.Ile1698Asn) c.4988T>A (p.Ile1663Asn) | |
X | g.154928698T>A | CA414913975 | F8 | c.5092A>T (p.Ile1698Phe) c.4987A>T (p.Ile1663Phe) | |
X | g.154928698T>C | CA414913977 | F8 | c.5092A>G (p.Ile1698Val) c.4987A>G (p.Ile1663Val) | |
X | g.154928698T>G | CA414913978 | F8 | c.5092A>C (p.Ile1698Leu) c.4987A>C (p.Ile1663Leu) | |
X | g.154928699G>A | CA519718393 | F8 | c.5091C>T (p.Asp1697=) c.4986C>T (p.Asp1662=) | |
X | g.154928699G>C | CA414913981 | F8 | c.5091C>G (p.Asp1697Glu) c.4986C>G (p.Asp1662Glu) | |
X | g.154928699G>T | CA414913983 | F8 | c.5091C>A (p.Asp1697Glu) c.4986C>A (p.Asp1662Glu) | |
X | g.154928700T>A | CA414913985 | F8 | c.5090A>T (p.Asp1697Val) c.4985A>T (p.Asp1662Val) | |
X | g.154928700T>C | CA10568040 | F8 | c.5090A>G (p.Asp1697Gly) c.4985A>G (p.Asp1662Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154928700T>G | CA414913988 | F8 | c.5090A>C (p.Asp1697Ala) c.4985A>C (p.Asp1662Ala) | |
X | g.154928700T= | CA2466835773 | F8 | c.5090A= (p.Asp1697=) c.4985A= (p.Asp1662=) | |
X | g.154928701C>A | CA414913990 | F8 | c.5089G>T (p.Asp1697Tyr) c.4984G>T (p.Asp1662Tyr) | |
X | g.154928701C= | CA2466835774 | F8 | c.5089G= (p.Asp1697=) c.4984G= (p.Asp1662=) | |
X | g.154928701C>G | CA414913992 | F8 | c.5089G>C (p.Asp1697His) c.4984G>C (p.Asp1662His) | |
X | g.154928701C>T | CA414913994 | F8 | c.5089G>A (p.Asp1697Asn) c.4984G>A (p.Asp1662Asn) | dbSNP |
X | g.154928702A>C | CA414913997 | F8 | c.5088T>G (p.Phe1696Leu) c.4983T>G (p.Phe1661Leu) | gnomAD v4 |
X | g.154928702A>G | CA519718394 | F8 | c.5088T>C (p.Phe1696=) c.4983T>C (p.Phe1661=) | |
X | g.154928702A>T | CA414913998 | F8 | c.5088T>A (p.Phe1696Leu) c.4983T>A (p.Phe1661Leu) | |
X | g.154928705dup | CA2466835775 | F8 | c.5088dup (p.Asp1697Ter) c.4983dup (p.Asp1662Ter) | dbSNP |
X | g.154928703A>C | CA414914002 | F8 | c.5087T>G (p.Phe1696Cys) c.4982T>G (p.Phe1661Cys) | |
X | g.154928703A>G | CA414914003 | F8 | c.5087T>C (p.Phe1696Ser) c.4982T>C (p.Phe1661Ser) | |
X | g.154928703A>T | CA414914000 | F8 | c.5087T>A (p.Phe1696Tyr) c.4982T>A (p.Phe1661Tyr) | |
X | g.154928703_154928706del | CA2695237929 | F8 | c.5084_5087del (p.Asp1695ValfsTer?) c.4979_4982del (p.Asp1660ValfsTer?) | |
X | g.154928704A>C | CA414914005 | F8 | c.5086T>G (p.Phe1696Val) c.4981T>G (p.Phe1661Val) | |
X | g.154928704A>G | CA414914007 | F8 | c.5086T>C (p.Phe1696Leu) c.4981T>C (p.Phe1661Leu) | |
X | g.154928704A>T | CA414914008 | F8 | c.5086T>A (p.Phe1696Ile) c.4981T>A (p.Phe1661Ile) | |
X | g.154928705A= | CA2466835776 | F8 | c.5085T= (p.Asp1695=) c.4980T= (p.Asp1660=) | |
X | g.154928705A>C | CA414914011 | F8 | c.5085T>G (p.Asp1695Glu) c.4980T>G (p.Asp1660Glu) | |
X | g.154928705A>G | CA519718395 | F8 | c.5085T>C (p.Asp1695=) c.4980T>C (p.Asp1660=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154928705A>T | CA414914013 | F8 | c.5085T>A (p.Asp1695Glu) c.4980T>A (p.Asp1660Glu) | |
X | g.154928706T>A | CA414914014 | F8 | c.5084A>T (p.Asp1695Val) c.4979A>T (p.Asp1660Val) | |
X | g.154928706T>C | CA414914016 | F8 | c.5084A>G (p.Asp1695Gly) c.4979A>G (p.Asp1660Gly) | |
X | g.154928706T>G | CA414914018 | F8 | c.5084A>C (p.Asp1695Ala) c.4979A>C (p.Asp1660Ala) | |
X | g.154928707C>A | CA414914019 | F8 | c.5083G>T (p.Asp1695Tyr) c.4978G>T (p.Asp1660Tyr) | |
X | g.154928707C>G | CA414914020 | F8 | c.5083G>C (p.Asp1695His) c.4978G>C (p.Asp1660His) | |
X | g.154928707C>T | CA414914021 | F8 | c.5083G>A (p.Asp1695Asn) c.4978G>A (p.Asp1660Asn) | |
X | g.154928708T>A | CA414914023 | F8 | c.5082A>T (p.Glu1694Asp) c.4977A>T (p.Glu1659Asp) | |
X | g.154928708T>C | CA519718396 | F8 | c.5082A>G (p.Glu1694=) c.4977A>G (p.Glu1659=) | |
X | g.154928708T>G | CA414914022 | F8 | c.5082A>C (p.Glu1694Asp) c.4977A>C (p.Glu1659Asp) | |
X | g.154928709T>A | CA414914024 | F8 | c.5081A>T (p.Glu1694Val) c.4976A>T (p.Glu1659Val) | |
X | g.154928709T>C | CA414914025 | F8 | c.5081A>G (p.Glu1694Gly) c.4976A>G (p.Glu1659Gly) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154928709T>G | CA414914026 | F8 | c.5081A>C (p.Glu1694Ala) c.4976A>C (p.Glu1659Ala) | |
X | g.154928709T= | CA2466835777 | F8 | c.5081A= (p.Glu1694=) c.4976A= (p.Glu1659=) | |
X | g.154928710C>A | CA414914029 | F8 | c.5080G>T (p.Glu1694Ter) c.4975G>T (p.Glu1659Ter) | dbSNP |
X | g.154928710C= | CA2466835778 | F8 | c.5080G= (p.Glu1694=) c.4975G= (p.Glu1659=) | |
X | g.154928710C>G | CA337327071 | F8 | c.5080G>C (p.Glu1694Gln) c.4975G>C (p.Glu1659Gln) | dbSNP gnomAD v3 gnomAD v4 |
X | g.154928710C>T | CA414914030 | F8 | c.5080G>A (p.Glu1694Lys) c.4975G>A (p.Glu1659Lys) | |
X | g.154928711C>A | CA414914032 | F8 | c.5079G>T (p.Lys1693Asn) c.4974G>T (p.Lys1658Asn) | |
X | g.154928711C>G | CA414914034 | F8 | c.5079G>C (p.Lys1693Asn) c.4974G>C (p.Lys1658Asn) | |
X | g.154928711C>T | CA519718397 | F8 | c.5079G>A (p.Lys1693=) c.4974G>A (p.Lys1658=) | |
X | g.154928712T>A | CA414914036 | F8 | c.5078A>T (p.Lys1693Met) c.4973A>T (p.Lys1658Met) | |
X | g.154928712T>C | CA414914038 | F8 | c.5078A>G (p.Lys1693Arg) c.4973A>G (p.Lys1658Arg) | |
X | g.154928712T>G | CA414914040 | F8 | c.5078A>C (p.Lys1693Thr) c.4973A>C (p.Lys1658Thr) | |
X | g.154928713del | CA2695237932 | F8 | c.5078del (p.Lys1693ArgfsTer?) c.4973del (p.Lys1658ArgfsTer?) | |
X | g.154928713T>A | CA414914046 | F8 | c.5077A>T (p.Lys1693Ter) c.4972A>T (p.Lys1658Ter) | |
X | g.154928713T>C | CA414914042 | F8 | c.5077A>G (p.Lys1693Glu) c.4972A>G (p.Lys1658Glu) | |
X | g.154928713T>G | CA414914044 | F8 | c.5077A>C (p.Lys1693Gln) c.4972A>C (p.Lys1658Gln) | |
X | g.154928714C>A | CA414914048 | F8 | c.5076G>T (p.Lys1692Asn) c.4971G>T (p.Lys1657Asn) | |
X | g.154928714C= | CA2466835779 | F8 | c.5076G= (p.Lys1692=) c.4971G= (p.Lys1657=) | |
X | g.154928714C>G | CA414914050 | F8 | c.5076G>C (p.Lys1692Asn) c.4971G>C (p.Lys1657Asn) | |
X | g.154928714C>T | CA519718398 | F8 | c.5076G>A (p.Lys1692=) c.4971G>A (p.Lys1657=) | dbSNP |
X | g.154928714_154928719delinsCTTCAT | CA2466835780 | F8 | c.5071_5076delinsATGAAG (p.Met1691=) c.4966_4971delinsATGAAG (p.Met1656=) | |
X | g.154928715T>A | CA414914052 | F8 | c.5075A>T (p.Lys1692Met) c.4970A>T (p.Lys1657Met) | |
X | g.154928715T>C | CA337327078 | F8 | c.5075A>G (p.Lys1692Arg) c.4970A>G (p.Lys1657Arg) | dbSNP |
X | g.154928715T>G | CA414914053 | F8 | c.5075A>C (p.Lys1692Thr) c.4970A>C (p.Lys1657Thr) | |
X | g.154928715T= | CA2466835782 | F8 | c.5075A= (p.Lys1692=) c.4970A= (p.Lys1657=) | |
X | g.154928719_154928723del | CA2466835781 | F8 | c.5071_5075del (p.Met1691GlufsTer5) c.4966_4970del (p.Met1656GlufsTer5) | dbSNP |
X | g.154928716T>A | CA414914057 | F8 | c.5074A>T (p.Lys1692Ter) c.4969A>T (p.Lys1657Ter) | |
X | g.154928716T>C | CA414914059 | F8 | c.5074A>G (p.Lys1692Glu) c.4969A>G (p.Lys1657Glu) | |
X | g.154928716T>G | CA414914061 | F8 | c.5074A>C (p.Lys1692Gln) c.4969A>C (p.Lys1657Gln) | |
X | g.154928717C>A | CA414914063 | F8 | c.5073G>T (p.Met1691Ile) c.4968G>T (p.Met1656Ile) | gnomAD v4 |
X | g.154928717C>G | CA414914065 | F8 | c.5073G>C (p.Met1691Ile) c.4968G>C (p.Met1656Ile) | |
X | g.154928717C>T | CA414914067 | F8 | c.5073G>A (p.Met1691Ile) c.4968G>A (p.Met1656Ile) | |
X | g.154928718A>C | CA414914069 | F8 | c.5072T>G (p.Met1691Arg) c.4967T>G (p.Met1656Arg) | |
X | g.154928718A>G | CA414914070 | F8 | c.5072T>C (p.Met1691Thr) c.4967T>C (p.Met1656Thr) | |
X | g.154928718A>T | CA414914071 | F8 | c.5072T>A (p.Met1691Lys) c.4967T>A (p.Met1656Lys) | |
X | g.154928719T>A | CA414914072 | F8 | c.5071A>T (p.Met1691Leu) c.4966A>T (p.Met1656Leu) | |
X | g.154928719T>C | CA414914073 | F8 | c.5071A>G (p.Met1691Val) c.4966A>G (p.Met1656Val) | |
X | g.154928719T>G | CA414914074 | F8 | c.5071A>C (p.Met1691Leu) c.4966A>C (p.Met1656Leu) | |
X | g.154928720T>A | CA414914076 | F8 | c.5070A>T (p.Glu1690Asp) c.4965A>T (p.Glu1655Asp) | |
X | g.154928720T>C | CA519718399 | F8 | c.5070A>G (p.Glu1690=) c.4965A>G (p.Glu1655=) | |
X | g.154928720T>G | CA414914075 | F8 | c.5070A>C (p.Glu1690Asp) c.4965A>C (p.Glu1655Asp) | |
X | g.154928720_154928731delinsCA | CA2695237933 | F8 | c.5059_5070delinsTG (p.Ile1687Ter) c.4954_4965delinsTG (p.Ile1652Ter) | |
X | g.154928721T>A | CA414914078 | F8 | c.5069A>T (p.Glu1690Val) c.4964A>T (p.Glu1655Val) | |
X | g.154928721T>C | CA10568041 | F8 | c.5069A>G (p.Glu1690Gly) c.4964A>G (p.Glu1655Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154928721T>G | CA414914079 | F8 | c.5069A>C (p.Glu1690Ala) c.4964A>C (p.Glu1655Ala) | |
X | g.154928721T= | CA2466835783 | F8 | c.5069A= (p.Glu1690=) c.4964A= (p.Glu1655=) | |
X | g.154928722C>A | CA414914082 | F8 | c.5068G>T (p.Glu1690Ter) c.4963G>T (p.Glu1655Ter) | COSMIC COSMIC |
X | g.154928722C= | CA2466835784 | F8 | c.5068G= (p.Glu1690=) c.4963G= (p.Glu1655=) | |
X | g.154928722C>G | CA414914084 | F8 | c.5068G>C (p.Glu1690Gln) c.4963G>C (p.Glu1655Gln) | |
X | g.154928722C>T | CA414914086 | F8 | c.5068G>A (p.Glu1690Lys) c.4963G>A (p.Glu1655Lys) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154928723A>C | CA519718400 | F8 | c.5067T>G (p.Val1689=) c.4962T>G (p.Val1654=) | |
X | g.154928723A>G | CA519718401 | F8 | c.5067T>C (p.Val1689=) c.4962T>C (p.Val1654=) | |
X | g.154928723A>T | CA519718402 | F8 | c.5067T>A (p.Val1689=) c.4962T>A (p.Val1654=) | |
X | g.154928724A>C | CA414914089 | F8 | c.5066T>G (p.Val1689Gly) c.4961T>G (p.Val1654Gly) | |
X | g.154928724A>G | CA414914091 | F8 | c.5066T>C (p.Val1689Ala) c.4961T>C (p.Val1654Ala) | |
X | g.154928724A>T | CA414914092 | F8 | c.5066T>A (p.Val1689Asp) c.4961T>A (p.Val1654Asp) | |
X | g.154928725C>A | CA414914094 | F8 | c.5065G>T (p.Val1689Phe) c.4960G>T (p.Val1654Phe) | |
X | g.154928725C>G | CA414914099 | F8 | c.5065G>C (p.Val1689Leu) c.4960G>C (p.Val1654Leu) | |
X | g.154928725C>T | CA414914100 | F8 | c.5065G>A (p.Val1689Ile) c.4960G>A (p.Val1654Ile) | |
X | g.154928726T>A | CA519718403 | F8 | c.5064A>T (p.Ser1688=) c.4959A>T (p.Ser1653=) | |
X | g.154928726T>C | CA519718404 | F8 | c.5064A>G (p.Ser1688=) c.4959A>G (p.Ser1653=) | |
X | g.154928726T>G | CA519718405 | F8 | c.5064A>C (p.Ser1688=) c.4959A>C (p.Ser1653=) | |
X | g.154928727G>A | CA10568042 | F8 | c.5063C>T (p.Ser1688Leu) c.4958C>T (p.Ser1653Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154928727G>C | CA414914106 | F8 | c.5063C>G (p.Ser1688Ter) c.4958C>G (p.Ser1653Ter) | |
X | g.154928727G= | CA2466835785 | F8 | c.5063C= (p.Ser1688=) c.4958C= (p.Ser1653=) | |
X | g.154928727G>T | CA414914104 | F8 | c.5063C>A (p.Ser1688Ter) c.4958C>A (p.Ser1653Ter) | |
X | g.154928728A>C | CA414914109 | F8 | c.5062T>G (p.Ser1688Ala) c.4957T>G (p.Ser1653Ala) | |
X | g.154928728A>G | CA414914111 | F8 | c.5062T>C (p.Ser1688Pro) c.4957T>C (p.Ser1653Pro) | |
X | g.154928728A>T | CA414914114 | F8 | c.5062T>A (p.Ser1688Thr) c.4957T>A (p.Ser1653Thr) | |
X | g.154928730_154928731del | CA2695237936 | F8 | c.5061_5062del (p.Val1689Ter) c.4956_4957del (p.Val1654Ter) | |
X | g.154928729T>A | CA519718406 | F8 | c.5061A>T (p.Ile1687=) c.4956A>T (p.Ile1652=) | |
X | g.154928729T>C | CA10568043 | F8 | c.5061A>G (p.Ile1687Met) c.4956A>G (p.Ile1652Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154928729T>G | CA519718407 | F8 | c.5061A>C (p.Ile1687=) c.4956A>C (p.Ile1652=) | |
X | g.154928729T= | CA2466835786 | F8 | c.5061A= (p.Ile1687=) c.4956A= (p.Ile1652=) | |
X | g.154928730A>C | CA414914118 | F8 | c.5060T>G (p.Ile1687Arg) c.4955T>G (p.Ile1652Arg) | |
X | g.154928730A>G | CA414914119 | F8 | c.5060T>C (p.Ile1687Thr) c.4955T>C (p.Ile1652Thr) | |
X | g.154928730A>T | CA414914121 | F8 | c.5060T>A (p.Ile1687Lys) c.4955T>A (p.Ile1652Lys) | |
X | g.154928731T>A | CA414914123 | F8 | c.5059A>T (p.Ile1687Leu) c.4954A>T (p.Ile1652Leu) | |
X | g.154928731T>C | CA414914125 | F8 | c.5059A>G (p.Ile1687Val) c.4954A>G (p.Ile1652Val) | dbSNP gnomAD v4 |
X | g.154928731T>G | CA414914127 | F8 | c.5059A>C (p.Ile1687Leu) c.4954A>C (p.Ile1652Leu) | gnomAD v4 |
X | g.154928731T= | CA2466835787 | F8 | c.5059A= (p.Ile1687=) c.4954A= (p.Ile1652=) | |
X | g.154928731_154928732del | CA2695237937 | F8 | c.5058_5059del (p.Val1689Ter) c.4953_4954del (p.Val1654Ter) | |
X | g.154928732G>A | CA519718408 | F8 | c.5058C>T (p.Thr1686=) c.4953C>T (p.Thr1651=) | dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
X | g.154928732G>C | CA519718410 | F8 | c.5058C>G (p.Thr1686=) c.4953C>G (p.Thr1651=) | |
X | g.154928732G= | CA2466835788 | F8 | c.5058C= (p.Thr1686=) c.4953C= (p.Thr1651=) | |
X | g.154928732G>T | CA519718409 | F8 | c.5058C>A (p.Thr1686=) c.4953C>A (p.Thr1651=) | |
X | g.154928733G>A | CA414914132 | F8 | c.5057C>T (p.Thr1686Ile) c.4952C>T (p.Thr1651Ile) | |
X | g.154928733G>C | CA414914130 | F8 | c.5057C>G (p.Thr1686Ser) c.4952C>G (p.Thr1651Ser) | |
X | g.154928733G>T | CA414914129 | F8 | c.5057C>A (p.Thr1686Asn) c.4952C>A (p.Thr1651Asn) | |
X | g.154928734T>A | CA414914134 | F8 | c.5056A>T (p.Thr1686Ser) c.4951A>T (p.Thr1651Ser) | |
X | g.154928734T>C | CA414914136 | F8 | c.5056A>G (p.Thr1686Ala) c.4951A>G (p.Thr1651Ala) | |
X | g.154928734T>G | CA414914138 | F8 | c.5056A>C (p.Thr1686Pro) c.4951A>C (p.Thr1651Pro) | |
X | g.154928735A>C | CA414914139 | F8 | c.5055T>G (p.Asp1685Glu) c.4950T>G (p.Asp1650Glu) | |
X | g.154928735A>G | CA519718411 | F8 | c.5055T>C (p.Asp1685=) c.4950T>C (p.Asp1650=) | |
X | g.154928735A>T | CA414914140 | F8 | c.5055T>A (p.Asp1685Glu) c.4950T>A (p.Asp1650Glu) | |
X | g.154928736T>A | CA414914142 | F8 | c.5054A>T (p.Asp1685Val) c.4949A>T (p.Asp1650Val) | |
X | g.154928736T>C | CA414914144 | F8 | c.5054A>G (p.Asp1685Gly) c.4949A>G (p.Asp1650Gly) | |
X | g.154928736T>G | CA414914146 | F8 | c.5054A>C (p.Asp1685Ala) c.4949A>C (p.Asp1650Ala) | |
X | g.154928737C>A | CA414914147 | F8 | c.5053G>T (p.Asp1685Tyr) c.4948G>T (p.Asp1650Tyr) | dbSNP |
X | g.154928737C>G | CA414914148 | F8 | c.5053G>C (p.Asp1685His) c.4948G>C (p.Asp1650His) | |
X | g.154928737C>T | CA414914150 | F8 | c.5053G>A (p.Asp1685Asn) c.4948G>A (p.Asp1650Asn) | gnomAD v4 |
X | g.154928738A= | CA2466835789 | F8 | c.5052T= (p.Asp1684=) c.4947T= (p.Asp1649=) | |
X | g.154928738A>C | CA414914152 | F8 | c.5052T>G (p.Asp1684Glu) c.4947T>G (p.Asp1649Glu) | |
X | g.154928738A>G | CA519718412 | F8 | c.5052T>C (p.Asp1684=) c.4947T>C (p.Asp1649=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154928738A>T | CA414914153 | F8 | c.5052T>A (p.Asp1684Glu) c.4947T>A (p.Asp1649Glu) | |
X | g.154928739T>A | CA414914154 | F8 | c.5051A>T (p.Asp1684Val) c.4946A>T (p.Asp1649Val) | |
X | g.154928739T>C | CA414914157 | F8 | c.5051A>G (p.Asp1684Gly) c.4946A>G (p.Asp1649Gly) | |
X | g.154928739T>G | CA414914155 | F8 | c.5051A>C (p.Asp1684Ala) c.4946A>C (p.Asp1649Ala) | |
X | g.154928740C>A | CA414914160 | F8 | c.5050G>T (p.Asp1684Tyr) c.4945G>T (p.Asp1649Tyr) | |
X | g.154928740C>G | CA414914161 | F8 | c.5050G>C (p.Asp1684His) c.4945G>C (p.Asp1649His) | |
X | g.154928740C>T | CA414914163 | F8 | c.5050G>A (p.Asp1684Asn) c.4945G>A (p.Asp1649Asn) | gnomAD v4 |
X | g.154928740_154928742delinsCAT | CA2466835790 | F8 | c.5048_5050delinsATG (p.Tyr1683=) c.4943_4945delinsATG (p.Tyr1648=) | |
X | g.154928741A= | CA2466835791 | F8 | c.5049T= (p.Tyr1683=) c.4944T= (p.Tyr1648=) | |
X | g.154928741A>C | CA414914165 | F8 | c.5049T>G (p.Tyr1683Ter) c.4944T>G (p.Tyr1648Ter) | |
X | g.154928741A>G | CA519718413 | F8 | c.5049T>C (p.Tyr1683=) c.4944T>C (p.Tyr1648=) | |
X | g.154928741A>T | CA414914167 | F8 | c.5049T>A (p.Tyr1683Ter) c.4944T>A (p.Tyr1648Ter) | dbSNP gnomAD v2 |
X | g.154928742_154928743del | CA873340403 | F8 | c.5048_5049del (p.Tyr1683Ter) c.4943_4944del (p.Tyr1648Ter) | dbSNP |
X | g.154928742T>A | CA414914169 | F8 | c.5048A>T (p.Tyr1683Phe) c.4943A>T (p.Tyr1648Phe) | gnomAD v4 |
X | g.154928742T>C | CA414914170 | F8 | c.5048A>G (p.Tyr1683Cys) c.4943A>G (p.Tyr1648Cys) | |
X | g.154928742T>G | CA414914172 | F8 | c.5048A>C (p.Tyr1683Ser) c.4943A>C (p.Tyr1648Ser) | |
X | g.154928743A>C | CA414914174 | F8 | c.5047T>G (p.Tyr1683Asp) c.4942T>G (p.Tyr1648Asp) | |
X | g.154928743A>G | CA414914176 | F8 | c.5047T>C (p.Tyr1683His) c.4942T>C (p.Tyr1648His) | |
X | g.154928743A>T | CA414914177 | F8 | c.5047T>A (p.Tyr1683Asn) c.4942T>A (p.Tyr1648Asn) | |
X | g.154928744del | CA2695237938 | F8 | c.5046del (p.Tyr1683MetfsTer9) c.4941del (p.Tyr1648MetfsTer9) | |
X | g.154928744G>A | CA519718414 | F8 | c.5046C>T (p.Asp1682=) c.4941C>T (p.Asp1647=) | |
X | g.154928744G>C | CA414914182 | F8 | c.5046C>G (p.Asp1682Glu) c.4941C>G (p.Asp1647Glu) | |
X | g.154928744G>T | CA414914180 | F8 | c.5046C>A (p.Asp1682Glu) c.4941C>A (p.Asp1647Glu) | |
X | g.154928745T>A | CA414914185 | F8 | c.5045A>T (p.Asp1682Val) c.4940A>T (p.Asp1647Val) | |
X | g.154928745T>C | CA414914186 | F8 | c.5045A>G (p.Asp1682Gly) c.4940A>G (p.Asp1647Gly) | |
X | g.154928745T>G | CA414914188 | F8 | c.5045A>C (p.Asp1682Ala) c.4940A>C (p.Asp1647Ala) | |
X | g.154928746C>A | CA414914190 | F8 | c.5044G>T (p.Asp1682Tyr) c.4939G>T (p.Asp1647Tyr) | |
X | g.154928746C>G | CA414914192 | F8 | c.5044G>C (p.Asp1682His) c.4939G>C (p.Asp1647His) | |
X | g.154928746C>T | CA414914193 | F8 | c.5044G>A (p.Asp1682Asn) c.4939G>A (p.Asp1647Asn) | |
X | g.154928747A>C | CA414914195 | F8 | c.5043T>G (p.Ile1681Met) c.4938T>G (p.Ile1646Met) | |
X | g.154928747A>G | CA519718415 | F8 | c.5043T>C (p.Ile1681=) c.4938T>C (p.Ile1646=) | |
X | g.154928747A>T | CA519718416 | F8 | c.5043T>A (p.Ile1681=) c.4938T>A (p.Ile1646=) | |
X | g.154928748A>C | CA414914197 | F8 | c.5042T>G (p.Ile1681Ser) c.4937T>G (p.Ile1646Ser) | |
X | g.154928748A>G | CA414914199 | F8 | c.5042T>C (p.Ile1681Thr) c.4937T>C (p.Ile1646Thr) | ClinVar |
X | g.154928748A>T | CA414914201 | F8 | c.5042T>A (p.Ile1681Asn) c.4937T>A (p.Ile1646Asn) | |
X | g.154928749T>A | CA414914206 | F8 | c.5041A>T (p.Ile1681Phe) c.4936A>T (p.Ile1646Phe) | |
X | g.154928749T>C | CA414914204 | F8 | c.5041A>G (p.Ile1681Val) c.4936A>G (p.Ile1646Val) | |
X | g.154928749T>G | CA414914203 | F8 | c.5041A>C (p.Ile1681Leu) c.4936A>C (p.Ile1646Leu) | |
X | g.154928751del | CA2695237939 | F8 | c.5041del (p.Ile1681LeufsTer11) c.4936del (p.Ile1646LeufsTer11) | |
X | g.154928750T>A | CA414914208 | F8 | c.5040A>T (p.Glu1680Asp) c.4935A>T (p.Glu1645Asp) | |
X | g.154928750T>C | CA519718417 | F8 | c.5040A>G (p.Glu1680=) c.4935A>G (p.Glu1645=) | |
X | g.154928750T>G | CA414914210 | F8 | c.5040A>C (p.Glu1680Asp) c.4935A>C (p.Glu1645Asp) | |
X | g.154928751T>A | CA414914213 | F8 | c.5039A>T (p.Glu1680Val) c.4934A>T (p.Glu1645Val) | |
X | g.154928751T>C | CA414914215 | F8 | c.5039A>G (p.Glu1680Gly) c.4934A>G (p.Glu1645Gly) | dbSNP |
X | g.154928751T>G | CA414914217 | F8 | c.5039A>C (p.Glu1680Ala) c.4934A>C (p.Glu1645Ala) | |
X | g.154928751T= | CA2466835792 | F8 | c.5039A= (p.Glu1680=) c.4934A= (p.Glu1645=) |