Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154904812_154905024del | CA2695238084 | F8 | c.5378_5586+4del c.5273_5481+4del | |
X | g.154904932C>A | CA414908767 | F8 | c.5465G>T (p.Arg1822Ile) c.5360G>T (p.Arg1787Ile) | |
X | g.154904932C>G | CA414908768 | F8 | c.5465G>C (p.Arg1822Thr) c.5360G>C (p.Arg1787Thr) | |
X | g.154904932C>T | CA414908769 | F8 | c.5465G>A (p.Arg1822Lys) c.5360G>A (p.Arg1787Lys) | |
X | g.154904932_154904933insA | CA519357427 | F8 | c.5464_5465insT (p.Arg1822MetfsTer8) c.5359_5360insT (p.Arg1787MetfsTer8) | |
X | g.154904933del | CA2695238138 | F8 | c.5464del (p.Arg1822GlufsTer?) c.5359del (p.Arg1787GlufsTer?) | |
X | g.154904933T>A | CA414908770 | F8 | c.5464A>T (p.Arg1822Ter) c.5359A>T (p.Arg1787Ter) | |
X | g.154904933T>C | CA414908771 | F8 | c.5464A>G (p.Arg1822Gly) c.5359A>G (p.Arg1787Gly) | |
X | g.154904933T>G | CA519357433 | F8 | c.5464A>C (p.Arg1822=) c.5359A>C (p.Arg1787=) | |
X | g.154904934A= | CA2466828458 | F8 | c.5463T= (p.Pro1821=) c.5358T= (p.Pro1786=) | |
X | g.154904934A>C | CA519357444 | F8 | c.5463T>G (p.Pro1821=) c.5358T>G (p.Pro1786=) | |
X | g.154904934A>G | CA519357441 | F8 | c.5463T>C (p.Pro1821=) c.5358T>C (p.Pro1786=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154904934A>T | CA519357438 | F8 | c.5463T>A (p.Pro1821=) c.5358T>A (p.Pro1786=) | |
X | g.154904935G>A | CA10567970 | F8 | c.5462C>T (p.Pro1821Leu) c.5357C>T (p.Pro1786Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154904935G>C | CA414908772 | F8 | c.5462C>G (p.Pro1821Arg) c.5357C>G (p.Pro1786Arg) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154904935G= | CA2466828459 | F8 | c.5462C= (p.Pro1821=) c.5357C= (p.Pro1786=) | |
X | g.154904935G>T | CA414908773 | F8 | c.5462C>A (p.Pro1821His) c.5357C>A (p.Pro1786His) | |
X | g.154904936G>A | CA414908774 | F8 | c.5461C>T (p.Pro1821Ser) c.5356C>T (p.Pro1786Ser) | |
X | g.154904936G>C | CA414908775 | F8 | c.5461C>G (p.Pro1821Ala) c.5356C>G (p.Pro1786Ala) | |
X | g.154904936G>T | CA414908776 | F8 | c.5461C>A (p.Pro1821Thr) c.5356C>A (p.Pro1786Thr) | gnomAD v4 COSMIC COSMIC |
X | g.154904937T>A | CA414908777 | F8 | c.5460A>T (p.Glu1820Asp) c.5355A>T (p.Glu1785Asp) | |
X | g.154904937T>C | CA519357454 | F8 | c.5460A>G (p.Glu1820=) c.5355A>G (p.Glu1785=) | |
X | g.154904937T>G | CA414908778 | F8 | c.5460A>C (p.Glu1820Asp) c.5355A>C (p.Glu1785Asp) | |
X | g.154904938del | CA2695238139 | F8 | c.5460del (p.Glu1820AspfsTer?) c.5355del (p.Glu1785AspfsTer?) | |
X | g.154904938T>A | CA414908779 | F8 | c.5459A>T (p.Glu1820Val) c.5354A>T (p.Glu1785Val) | |
X | g.154904938T>C | CA414908781 | F8 | c.5459A>G (p.Glu1820Gly) c.5354A>G (p.Glu1785Gly) | |
X | g.154904938T>G | CA414908780 | F8 | c.5459A>C (p.Glu1820Ala) c.5354A>C (p.Glu1785Ala) | |
X | g.154904939C>A | CA414908782 | F8 | c.5458G>T (p.Glu1820Ter) c.5353G>T (p.Glu1785Ter) | |
X | g.154904939C>G | CA414908783 | F8 | c.5458G>C (p.Glu1820Gln) c.5353G>C (p.Glu1785Gln) | |
X | g.154904939C>T | CA414908784 | F8 | c.5458G>A (p.Glu1820Lys) c.5353G>A (p.Glu1785Lys) | |
X | g.154904940T>A | CA519357459 | F8 | c.5457A>T (p.Ala1819=) c.5352A>T (p.Ala1784=) | |
X | g.154904940T>C | CA519357464 | F8 | c.5457A>G (p.Ala1819=) c.5352A>G (p.Ala1784=) | gnomAD v4 |
X | g.154904940T>G | CA519357461 | F8 | c.5457A>C (p.Ala1819=) c.5352A>C (p.Ala1784=) | |
X | g.154904941G>A | CA414908785 | F8 | c.5456C>T (p.Ala1819Val) c.5351C>T (p.Ala1784Val) | |
X | g.154904941G>C | CA414908786 | F8 | c.5456C>G (p.Ala1819Gly) c.5351C>G (p.Ala1784Gly) | |
X | g.154904941G>T | CA414908787 | F8 | c.5456C>A (p.Ala1819Glu) c.5351C>A (p.Ala1784Glu) | |
X | g.154904942C>A | CA414908788 | F8 | c.5455G>T (p.Ala1819Ser) c.5350G>T (p.Ala1784Ser) | |
X | g.154904942C>G | CA414908789 | F8 | c.5455G>C (p.Ala1819Pro) c.5350G>C (p.Ala1784Pro) | |
X | g.154904942C>T | CA414908790 | F8 | c.5455G>A (p.Ala1819Thr) c.5350G>A (p.Ala1784Thr) | gnomAD v4 |
X | g.154904943_154904944dup | CA2695238141 | F8 | c.5454_5455dup (p.Ala1819GlufsTer?) c.5349_5350dup (p.Ala1784GlufsTer?) | |
X | g.154904943T>A | CA519357477 | F8 | c.5454A>T (p.Gly1818=) c.5349A>T (p.Gly1783=) | |
X | g.154904943T>C | CA519357478 | F8 | c.5454A>G (p.Gly1818=) c.5349A>G (p.Gly1783=) | |
X | g.154904943T>G | CA519357480 | F8 | c.5454A>C (p.Gly1818=) c.5349A>C (p.Gly1783=) | |
X | g.154904944C>A | CA414908791 | F8 | c.5453G>T (p.Gly1818Val) c.5348G>T (p.Gly1783Val) | |
X | g.154904944C= | CA2466828460 | F8 | c.5453G= (p.Gly1818=) c.5348G= (p.Gly1783=) | |
X | g.154904944C>G | CA414908793 | F8 | c.5453G>C (p.Gly1818Ala) c.5348G>C (p.Gly1783Ala) | |
X | g.154904944C>T | CA414908792 | F8 | c.5453G>A (p.Gly1818Glu) c.5348G>A (p.Gly1783Glu) | dbSNP |
X | g.154904945dup | CA2825002936 | F8 | c.5453dup (p.Ala1819SerfsTer4) c.5348dup (p.Ala1784SerfsTer4) | ClinVar |
X | g.154904944_154905247delinsA | CA2580612537 | F8 | c.5374-224_5453delinsT c.5269-224_5348delinsT | ClinVar |
X | g.154904945C>A | CA414908794 | F8 | c.5452G>T (p.Gly1818Ter) c.5347G>T (p.Gly1783Ter) | |
X | g.154904945C>G | CA414908795 | F8 | c.5452G>C (p.Gly1818Arg) c.5347G>C (p.Gly1783Arg) | |
X | g.154904945C>T | CA414908796 | F8 | c.5452G>A (p.Gly1818Arg) c.5347G>A (p.Gly1783Arg) | |
X | g.154904946T>A | CA414908797 | F8 | c.5451A>T (p.Gln1817His) c.5346A>T (p.Gln1782His) | |
X | g.154904946T>C | CA519357496 | F8 | c.5451A>G (p.Gln1817=) c.5346A>G (p.Gln1782=) | |
X | g.154904946T>G | CA414908798 | F8 | c.5451A>C (p.Gln1817His) c.5346A>C (p.Gln1782His) | |
X | g.154904947T>A | CA414908799 | F8 | c.5450A>T (p.Gln1817Leu) c.5345A>T (p.Gln1782Leu) | |
X | g.154904947T>C | CA414908800 | F8 | c.5450A>G (p.Gln1817Arg) c.5345A>G (p.Gln1782Arg) | |
X | g.154904947T>G | CA414908801 | F8 | c.5450A>C (p.Gln1817Pro) c.5345A>C (p.Gln1782Pro) | |
X | g.154904948G>A | CA414908802 | F8 | c.5449C>T (p.Gln1817Ter) c.5344C>T (p.Gln1782Ter) | ClinVar dbSNP |
X | g.154904948G>C | CA414908803 | F8 | c.5449C>G (p.Gln1817Glu) c.5344C>G (p.Gln1782Glu) | |
X | g.154904948G>T | CA414908804 | F8 | c.5449C>A (p.Gln1817Lys) c.5344C>A (p.Gln1782Lys) | |
X | g.154904949C>A | CA414908805 | F8 | c.5448G>T (p.Arg1816Ser) c.5343G>T (p.Arg1781Ser) | dbSNP |
X | g.154904949C= | CA2466828461 | F8 | c.5448G= (p.Arg1816=) c.5343G= (p.Arg1781=) | |
X | g.154904949C>G | CA414908806 | F8 | c.5448G>C (p.Arg1816Ser) c.5343G>C (p.Arg1781Ser) | |
X | g.154904949C>T | CA519357511 | F8 | c.5448G>A (p.Arg1816=) c.5343G>A (p.Arg1781=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154904950C>A | CA414908807 | F8 | c.5447G>T (p.Arg1816Met) c.5342G>T (p.Arg1781Met) | |
X | g.154904950C>G | CA414908808 | F8 | c.5447G>C (p.Arg1816Thr) c.5342G>C (p.Arg1781Thr) | |
X | g.154904950C>T | CA414908809 | F8 | c.5447G>A (p.Arg1816Lys) c.5342G>A (p.Arg1781Lys) | |
X | g.154904951T>A | CA414908810 | F8 | c.5446A>T (p.Arg1816Trp) c.5341A>T (p.Arg1781Trp) | |
X | g.154904951T>C | CA414908811 | F8 | c.5446A>G (p.Arg1816Gly) c.5341A>G (p.Arg1781Gly) | |
X | g.154904951T>G | CA519357524 | F8 | c.5446A>C (p.Arg1816=) c.5341A>C (p.Arg1781=) | |
X | g.154904952C>A | CA414908812 | F8 | c.5445G>T (p.Gln1815His) c.5340G>T (p.Gln1780His) | |
X | g.154904952C>G | CA414908813 | F8 | c.5445G>C (p.Gln1815His) c.5340G>C (p.Gln1780His) | |
X | g.154904952C>T | CA519357529 | F8 | c.5445G>A (p.Gln1815=) c.5340G>A (p.Gln1780=) | |
X | g.154904953T>A | CA414908814 | F8 | c.5444A>T (p.Gln1815Leu) c.5339A>T (p.Gln1780Leu) | |
X | g.154904953T>C | CA414908815 | F8 | c.5444A>G (p.Gln1815Arg) c.5339A>G (p.Gln1780Arg) | dbSNP |
X | g.154904953T>G | CA414908816 | F8 | c.5444A>C (p.Gln1815Pro) c.5339A>C (p.Gln1780Pro) | |
X | g.154904953T= | CA2466828462 | F8 | c.5444A= (p.Gln1815=) c.5339A= (p.Gln1780=) | |
X | g.154904954G>A | CA255167 | F8 | c.5443C>T (p.Gln1815Ter) c.5338C>T (p.Gln1780Ter) | ClinVar dbSNP |
X | g.154904954G>C | CA414908818 | F8 | c.5443C>G (p.Gln1815Glu) c.5338C>G (p.Gln1780Glu) | |
X | g.154904954G= | CA2466828463 | F8 | c.5443C= (p.Gln1815=) c.5338C= (p.Gln1780=) | |
X | g.154904954G>T | CA414908817 | F8 | c.5443C>A (p.Gln1815Lys) c.5338C>A (p.Gln1780Lys) | |
X | g.154904955A>C | CA414908820 | F8 | c.5442T>G (p.Asp1814Glu) c.5337T>G (p.Asp1779Glu) | |
X | g.154904955A>G | CA519357543 | F8 | c.5442T>C (p.Asp1814=) c.5337T>C (p.Asp1779=) | |
X | g.154904955A>T | CA414908819 | F8 | c.5442T>A (p.Asp1814Glu) c.5337T>A (p.Asp1779Glu) | |
X | g.154904956T>A | CA414908821 | F8 | c.5441A>T (p.Asp1814Val) c.5336A>T (p.Asp1779Val) | ClinVar dbSNP |
X | g.154904956T>C | CA414908822 | F8 | c.5441A>G (p.Asp1814Gly) c.5336A>G (p.Asp1779Gly) | COSMIC COSMIC |
X | g.154904956T>G | CA414908823 | F8 | c.5441A>C (p.Asp1814Ala) c.5336A>C (p.Asp1779Ala) | |
X | g.154904956T= | CA2466828464 | F8 | c.5441A= (p.Asp1814=) c.5336A= (p.Asp1779=) | |
X | g.154904957C>A | CA414908824 | F8 | c.5440G>T (p.Asp1814Tyr) c.5335G>T (p.Asp1779Tyr) | |
X | g.154904957C>G | CA414908825 | F8 | c.5440G>C (p.Asp1814His) c.5335G>C (p.Asp1779His) | |
X | g.154904957C>T | CA414908826 | F8 | c.5440G>A (p.Asp1814Asn) c.5335G>A (p.Asp1779Asn) | |
X | g.154904958T>A | CA414908827 | F8 | c.5439A>T (p.Glu1813Asp) c.5334A>T (p.Glu1778Asp) | |
X | g.154904958T>C | CA519357559 | F8 | c.5439A>G (p.Glu1813=) c.5334A>G (p.Glu1778=) | |
X | g.154904958T>G | CA414908828 | F8 | c.5439A>C (p.Glu1813Asp) c.5334A>C (p.Glu1778Asp) | |
X | g.154904959T>A | CA414908830 | F8 | c.5438A>T (p.Glu1813Val) c.5333A>T (p.Glu1778Val) | |
X | g.154904959T>C | CA414908831 | F8 | c.5438A>G (p.Glu1813Gly) c.5333A>G (p.Glu1778Gly) | |
X | g.154904959T>G | CA414908832 | F8 | c.5438A>C (p.Glu1813Ala) c.5333A>C (p.Glu1778Ala) | |
X | g.154904960C>A | CA414908835 | F8 | c.5437G>T (p.Glu1813Ter) c.5332G>T (p.Glu1778Ter) | |
X | g.154904960C>G | CA414908833 | F8 | c.5437G>C (p.Glu1813Gln) c.5332G>C (p.Glu1778Gln) | |
X | g.154904960C>T | CA414908834 | F8 | c.5437G>A (p.Glu1813Lys) c.5332G>A (p.Glu1778Lys) | gnomAD v4 |
X | g.154904961C>A | CA414908836 | F8 | c.5436G>T (p.Glu1812Asp) c.5331G>T (p.Glu1777Asp) | |
X | g.154904961C>G | CA414908837 | F8 | c.5436G>C (p.Glu1812Asp) c.5331G>C (p.Glu1777Asp) | |
X | g.154904961C>T | CA519357572 | F8 | c.5436G>A (p.Glu1812=) c.5331G>A (p.Glu1777=) | COSMIC COSMIC |
X | g.154904962T>A | CA414908838 | F8 | c.5435A>T (p.Glu1812Val) c.5330A>T (p.Glu1777Val) | |
X | g.154904962T>C | CA414908839 | F8 | c.5435A>G (p.Glu1812Gly) c.5330A>G (p.Glu1777Gly) | |
X | g.154904962T>G | CA414908840 | F8 | c.5435A>C (p.Glu1812Ala) c.5330A>C (p.Glu1777Ala) | |
X | g.154904963C>A | CA414908841 | F8 | c.5434G>T (p.Glu1812Ter) c.5329G>T (p.Glu1777Ter) | dbSNP |
X | g.154904963C= | CA2466828465 | F8 | c.5434G= (p.Glu1812=) c.5329G= (p.Glu1777=) | |
X | g.154904963C>G | CA414908842 | F8 | c.5434G>C (p.Glu1812Gln) c.5329G>C (p.Glu1777Gln) | |
X | g.154904963C>T | CA10567971 | F8 | c.5434G>A (p.Glu1812Lys) c.5329G>A (p.Glu1777Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154904964A= | CA2466828466 | F8 | c.5433T= (p.Tyr1811=) c.5328T= (p.Tyr1776=) | |
X | g.154904964A>C | CA414908843 | F8 | c.5433T>G (p.Tyr1811Ter) c.5328T>G (p.Tyr1776Ter) | |
X | g.154904964A>G | CA519357588 | F8 | c.5433T>C (p.Tyr1811=) c.5328T>C (p.Tyr1776=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154904964A>T | CA414908844 | F8 | c.5433T>A (p.Tyr1811Ter) c.5328T>A (p.Tyr1776Ter) | |
X | g.154904965T>A | CA414908848 | F8 | c.5432A>T (p.Tyr1811Phe) c.5327A>T (p.Tyr1776Phe) | |
X | g.154904965T>C | CA414908846 | F8 | c.5432A>G (p.Tyr1811Cys) c.5327A>G (p.Tyr1776Cys) | |
X | g.154904965T>G | CA414908845 | F8 | c.5432A>C (p.Tyr1811Ser) c.5327A>C (p.Tyr1776Ser) | gnomAD v4 |
X | g.154904966A>C | CA414908857 | F8 | c.5431T>G (p.Tyr1811Asp) c.5326T>G (p.Tyr1776Asp) | |
X | g.154904966A>G | CA414908859 | F8 | c.5431T>C (p.Tyr1811His) c.5326T>C (p.Tyr1776His) | |
X | g.154904966A>T | CA414908861 | F8 | c.5431T>A (p.Tyr1811Asn) c.5326T>A (p.Tyr1776Asn) | |
X | g.154904967A= | CA2466828467 | F8 | c.5430T= (p.Ser1810=) c.5325T= (p.Ser1775=) | |
X | g.154904967A>C | CA10567972 | F8 | c.5430T>G (p.Ser1810=) c.5325T>G (p.Ser1775=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154904967A>G | CA519357602 | F8 | c.5430T>C (p.Ser1810=) c.5325T>C (p.Ser1775=) | |
X | g.154904967A>T | CA519357605 | F8 | c.5430T>A (p.Ser1810=) c.5325T>A (p.Ser1775=) | gnomAD v4 |
X | g.154904968G>A | CA414908868 | F8 | c.5429C>T (p.Ser1810Phe) c.5324C>T (p.Ser1775Phe) | |
X | g.154904968G>C | CA414908870 | F8 | c.5429C>G (p.Ser1810Cys) c.5324C>G (p.Ser1775Cys) | |
X | g.154904968G>T | CA414908871 | F8 | c.5429C>A (p.Ser1810Tyr) c.5324C>A (p.Ser1775Tyr) | |
X | g.154904969A>C | CA414908874 | F8 | c.5428T>G (p.Ser1810Ala) c.5323T>G (p.Ser1775Ala) | |
X | g.154904969A>G | CA414908876 | F8 | c.5428T>C (p.Ser1810Pro) c.5323T>C (p.Ser1775Pro) | COSMIC COSMIC |
X | g.154904969A>T | CA414908879 | F8 | c.5428T>A (p.Ser1810Thr) c.5323T>A (p.Ser1775Thr) | |
X | g.154904971del | CA2695238148 | F8 | c.5428del (p.Ser1810LeufsTer?) c.5323del (p.Ser1775LeufsTer?) | |
X | g.154904970A= | CA2466828468 | F8 | c.5427T= (p.Ile1809=) c.5322T= (p.Ile1774=) | |
X | g.154904970A>C | CA414908880 | F8 | c.5427T>G (p.Ile1809Met) c.5322T>G (p.Ile1774Met) | |
X | g.154904970A>G | CA10567973 | F8 | c.5427T>C (p.Ile1809=) c.5322T>C (p.Ile1774=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154904970A>T | CA519357619 | F8 | c.5427T>A (p.Ile1809=) c.5322T>A (p.Ile1774=) | COSMIC COSMIC |
X | g.154904971A>C | CA414908883 | F8 | c.5426T>G (p.Ile1809Ser) c.5321T>G (p.Ile1774Ser) | |
X | g.154904971A>G | CA414908881 | F8 | c.5426T>C (p.Ile1809Thr) c.5321T>C (p.Ile1774Thr) | |
X | g.154904971A>T | CA414908882 | F8 | c.5426T>A (p.Ile1809Asn) c.5321T>A (p.Ile1774Asn) | |
X | g.154904972T>A | CA414908885 | F8 | c.5425A>T (p.Ile1809Phe) c.5320A>T (p.Ile1774Phe) | |
X | g.154904972T>C | CA414908886 | F8 | c.5425A>G (p.Ile1809Val) c.5320A>G (p.Ile1774Val) | gnomAD v4 |
X | g.154904972T>G | CA414908888 | F8 | c.5425A>C (p.Ile1809Leu) c.5320A>C (p.Ile1774Leu) | |
X | g.154904973A>C | CA519357631 | F8 | c.5424T>G (p.Leu1808=) c.5319T>G (p.Leu1773=) | |
X | g.154904973A>G | CA519357633 | F8 | c.5424T>C (p.Leu1808=) c.5319T>C (p.Leu1773=) | |
X | g.154904973A>T | CA519357636 | F8 | c.5424T>A (p.Leu1808=) c.5319T>A (p.Leu1773=) | |
X | g.154904974A= | CA2466828469 | F8 | c.5423T= (p.Leu1808=) c.5318T= (p.Leu1773=) | |
X | g.154904974A>C | CA414908890 | F8 | c.5423T>G (p.Leu1808Arg) c.5318T>G (p.Leu1773Arg) | |
X | g.154904974A>G | CA10567974 | F8 | c.5423T>C (p.Leu1808Pro) c.5318T>C (p.Leu1773Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154904974A>T | CA414908891 | F8 | c.5423T>A (p.Leu1808His) c.5318T>A (p.Leu1773His) | |
X | g.154904975G>A | CA255166 | F8 | c.5422C>T (p.Leu1808Phe) c.5317C>T (p.Leu1773Phe) | ClinVar dbSNP |
X | g.154904975G>C | CA414908893 | F8 | c.5422C>G (p.Leu1808Val) c.5317C>G (p.Leu1773Val) | gnomAD v4 |
X | g.154904975G= | CA2466828470 | F8 | c.5422C= (p.Leu1808=) c.5317C= (p.Leu1773=) | |
X | g.154904975G>T | CA414908895 | F8 | c.5422C>A (p.Leu1808Ile) c.5317C>A (p.Leu1773Ile) | COSMIC COSMIC |
X | g.154904976del | CA2695238153 | F8 | c.5422del (p.Ile1809PhefsTer?) c.5317del (p.Ile1774PhefsTer?) | |
X | g.154904976G>A | CA519357650 | F8 | c.5421C>T (p.Ser1807=) c.5316C>T (p.Ser1772=) | dbSNP |
X | g.154904976G>C | CA414908899 | F8 | c.5421C>G (p.Ser1807Arg) c.5316C>G (p.Ser1772Arg) | dbSNP |
X | g.154904976G= | CA2466828471 | F8 | c.5421C= (p.Ser1807=) c.5316C= (p.Ser1772=) | |
X | g.154904976G>T | CA414908900 | F8 | c.5421C>A (p.Ser1807Arg) c.5316C>A (p.Ser1772Arg) | |
X | g.154904977C>A | CA414908903 | F8 | c.5420G>T (p.Ser1807Ile) c.5315G>T (p.Ser1772Ile) | |
X | g.154904977C>G | CA414908904 | F8 | c.5420G>C (p.Ser1807Thr) c.5315G>C (p.Ser1772Thr) | |
X | g.154904977C>T | CA414908902 | F8 | c.5420G>A (p.Ser1807Asn) c.5315G>A (p.Ser1772Asn) | |
X | g.154904978T>A | CA414908905 | F8 | c.5419A>T (p.Ser1807Cys) c.5314A>T (p.Ser1772Cys) | |
X | g.154904978T>C | CA414908907 | F8 | c.5419A>G (p.Ser1807Gly) c.5314A>G (p.Ser1772Gly) | |
X | g.154904978T>G | CA414908908 | F8 | c.5419A>C (p.Ser1807Arg) c.5314A>C (p.Ser1772Arg) | |
X | g.154904979A>C | CA519357662 | F8 | c.5418T>G (p.Ser1806=) c.5313T>G (p.Ser1771=) | |
X | g.154904979A>G | CA519357664 | F8 | c.5418T>C (p.Ser1806=) c.5313T>C (p.Ser1771=) | |
X | g.154904979A>T | CA519357666 | F8 | c.5418T>A (p.Ser1806=) c.5313T>A (p.Ser1771=) | |
X | g.154904980G>A | CA414908914 | F8 | c.5417C>T (p.Ser1806Phe) c.5312C>T (p.Ser1771Phe) | ClinVar dbSNP |
X | g.154904980G>C | CA414908915 | F8 | c.5417C>G (p.Ser1806Cys) c.5312C>G (p.Ser1771Cys) | |
X | g.154904980G= | CA2466828472 | F8 | c.5417C= (p.Ser1806=) c.5312C= (p.Ser1771=) | |
X | g.154904980G>T | CA414908918 | F8 | c.5417C>A (p.Ser1806Tyr) c.5312C>A (p.Ser1771Tyr) | |
X | g.154904981A>C | CA414908926 | F8 | c.5416T>G (p.Ser1806Ala) c.5311T>G (p.Ser1771Ala) | |
X | g.154904981A>G | CA414908920 | F8 | c.5416T>C (p.Ser1806Pro) c.5311T>C (p.Ser1771Pro) | |
X | g.154904981A>T | CA414908923 | F8 | c.5416T>A (p.Ser1806Thr) c.5311T>A (p.Ser1771Thr) | |
X | g.154904982A>C | CA414908929 | F8 | c.5415T>G (p.Tyr1805Ter) c.5310T>G (p.Tyr1770Ter) | |
X | g.154904982A>G | CA519357671 | F8 | c.5415T>C (p.Tyr1805=) c.5310T>C (p.Tyr1770=) | |
X | g.154904982A>T | CA414908930 | F8 | c.5415T>A (p.Tyr1805Ter) c.5310T>A (p.Tyr1770Ter) | |
X | g.154904983T>A | CA414908934 | F8 | c.5414A>T (p.Tyr1805Phe) c.5309A>T (p.Tyr1770Phe) | dbSNP |
X | g.154904983T>C | CA414908936 | F8 | c.5414A>G (p.Tyr1805Cys) c.5309A>G (p.Tyr1770Cys) | |
X | g.154904983T>G | CA414908939 | F8 | c.5414A>C (p.Tyr1805Ser) c.5309A>C (p.Tyr1770Ser) | |
X | g.154904983T= | CA2466828473 | F8 | c.5414A= (p.Tyr1805=) c.5309A= (p.Tyr1770=) | |
X | g.154904984A>C | CA414908943 | F8 | c.5413T>G (p.Tyr1805Asp) c.5308T>G (p.Tyr1770Asp) | |
X | g.154904984A>G | CA414908949 | F8 | c.5413T>C (p.Tyr1805His) c.5308T>C (p.Tyr1770His) | |
X | g.154904984A>T | CA414908946 | F8 | c.5413T>A (p.Tyr1805Asn) c.5308T>A (p.Tyr1770Asn) | |
X | g.154904986_154904988del | CA2695238157 | F8 | c.5411_5413del (p.Phe1804del) c.5306_5308del (p.Phe1769del) | |
X | g.154904985G>A | CA519357673 | F8 | c.5412C>T (p.Phe1804=) c.5307C>T (p.Phe1769=) | |
X | g.154904985G>C | CA414908954 | F8 | c.5412C>G (p.Phe1804Leu) c.5307C>G (p.Phe1769Leu) | |
X | g.154904985G>T | CA414908962 | F8 | c.5412C>A (p.Phe1804Leu) c.5307C>A (p.Phe1769Leu) | |
X | g.154904986A>C | CA414908965 | F8 | c.5411T>G (p.Phe1804Cys) c.5306T>G (p.Phe1769Cys) | |
X | g.154904986A>G | CA414908966 | F8 | c.5411T>C (p.Phe1804Ser) c.5306T>C (p.Phe1769Ser) | |
X | g.154904986A>T | CA414908968 | F8 | c.5411T>A (p.Phe1804Tyr) c.5306T>A (p.Phe1769Tyr) | |
X | g.154904987A>C | CA414908970 | F8 | c.5410T>G (p.Phe1804Val) c.5305T>G (p.Phe1769Val) | |
X | g.154904987A>G | CA414908973 | F8 | c.5410T>C (p.Phe1804Leu) c.5305T>C (p.Phe1769Leu) | |
X | g.154904987A>T | CA414908975 | F8 | c.5410T>A (p.Phe1804Ile) c.5305T>A (p.Phe1769Ile) | |
X | g.154904988_154904990dup | CA2695238159 | F8 | c.5408_5410dup (p.Ser1803_Phe1804insSer) c.5303_5305dup (p.Ser1768_Phe1769insSer) | |
X | g.154904988G>A | CA519357674 | F8 | c.5409C>T (p.Ser1803=) c.5304C>T (p.Ser1768=) | |
X | g.154904988G>C | CA519357675 | F8 | c.5409C>G (p.Ser1803=) c.5304C>G (p.Ser1768=) | |
X | g.154904988G>T | CA519357676 | F8 | c.5409C>A (p.Ser1803=) c.5304C>A (p.Ser1768=) | |
X | g.154904989G>A | CA414908976 | F8 | c.5408C>T (p.Ser1803Phe) c.5303C>T (p.Ser1768Phe) | dbSNP |
X | g.154904989G>C | CA414908977 | F8 | c.5408C>G (p.Ser1803Cys) c.5303C>G (p.Ser1768Cys) | |
X | g.154904989G= | CA2466828474 | F8 | c.5408C= (p.Ser1803=) c.5303C= (p.Ser1768=) | |
X | g.154904989G>T | CA255165 | F8 | c.5408C>A (p.Ser1803Tyr) c.5303C>A (p.Ser1768Tyr) | ClinVar dbSNP |
X | g.154904990A>C | CA414908979 | F8 | c.5407T>G (p.Ser1803Ala) c.5302T>G (p.Ser1768Ala) | |
X | g.154904990A>G | CA414908987 | F8 | c.5407T>C (p.Ser1803Pro) c.5302T>C (p.Ser1768Pro) | |
X | g.154904990A>T | CA414908981 | F8 | c.5407T>A (p.Ser1803Thr) c.5302T>A (p.Ser1768Thr) | |
X | g.154904991A>C | CA414908989 | F8 | c.5406T>G (p.Tyr1802Ter) c.5301T>G (p.Tyr1767Ter) | |
X | g.154904991A>G | CA519357679 | F8 | c.5406T>C (p.Tyr1802=) c.5301T>C (p.Tyr1767=) | |
X | g.154904991A>T | CA414908991 | F8 | c.5406T>A (p.Tyr1802Ter) c.5301T>A (p.Tyr1767Ter) | |
X | g.154904992T>A | CA414908993 | F8 | c.5405A>T (p.Tyr1802Phe) c.5300A>T (p.Tyr1767Phe) | |
X | g.154904992T>C | CA414909004 | F8 | c.5405A>G (p.Tyr1802Cys) c.5300A>G (p.Tyr1767Cys) | ClinVar gnomAD v4 |
X | g.154904992T>G | CA414909007 | F8 | c.5405A>C (p.Tyr1802Ser) c.5300A>C (p.Tyr1767Ser) | |
X | g.154904992_154904993insCC | CA2695238164 | F8 | c.5404_5405insGG (p.Tyr1802TrpfsTer?) c.5299_5300insGG (p.Tyr1767TrpfsTer?) | |
X | g.154904993A>C | CA414909010 | F8 | c.5404T>G (p.Tyr1802Asp) c.5299T>G (p.Tyr1767Asp) | COSMIC COSMIC |
X | g.154904993A>G | CA414909013 | F8 | c.5404T>C (p.Tyr1802His) c.5299T>C (p.Tyr1767His) | |
X | g.154904993A>T | CA414909022 | F8 | c.5404T>A (p.Tyr1802Asn) c.5299T>A (p.Tyr1767Asn) | |
X | g.154904994G>A | CA519357683 | F8 | c.5403C>T (p.Pro1801=) c.5298C>T (p.Pro1766=) | |
X | g.154904994G>C | CA519357684 | F8 | c.5403C>G (p.Pro1801=) c.5298C>G (p.Pro1766=) | |
X | g.154904994G>T | CA519357685 | F8 | c.5403C>A (p.Pro1801=) c.5298C>A (p.Pro1766=) | |
X | g.154904995G>A | CA414909026 | F8 | c.5402C>T (p.Pro1801Leu) c.5297C>T (p.Pro1766Leu) | |
X | g.154904995G>C | CA414909028 | F8 | c.5402C>G (p.Pro1801Arg) c.5297C>G (p.Pro1766Arg) | |
X | g.154904995G>T | CA414909031 | F8 | c.5402C>A (p.Pro1801His) c.5297C>A (p.Pro1766His) | gnomAD v4 |
X | g.154904996G>A | CA414909037 | F8 | c.5401C>T (p.Pro1801Ser) c.5296C>T (p.Pro1766Ser) | COSMIC COSMIC |
X | g.154904996G>C | CA414909036 | F8 | c.5401C>G (p.Pro1801Ala) c.5296C>G (p.Pro1766Ala) | |
X | g.154904996G>T | CA414909033 | F8 | c.5401C>A (p.Pro1801Thr) c.5296C>A (p.Pro1766Thr) | |
X | g.154904997A>C | CA519357688 | F8 | c.5400T>G (p.Arg1800=) c.5295T>G (p.Arg1765=) | |
X | g.154904997A>G | CA519357687 | F8 | c.5400T>C (p.Arg1800=) c.5295T>C (p.Arg1765=) | |
X | g.154904997A>T | CA519357686 | F8 | c.5400T>A (p.Arg1800=) c.5295T>A (p.Arg1765=) | |
X | g.154904998C>A | CA414909041 | F8 | c.5399G>T (p.Arg1800Leu) c.5294G>T (p.Arg1765Leu) | |
X | g.154904998C= | CA2466828475 | F8 | c.5399G= (p.Arg1800=) c.5294G= (p.Arg1765=) | |
X | g.154904998C>G | CA414909043 | F8 | c.5399G>C (p.Arg1800Pro) c.5294G>C (p.Arg1765Pro) | |
X | g.154904998C>T | CA255162 | F8 | c.5399G>A (p.Arg1800His) c.5294G>A (p.Arg1765His) | ClinVar dbSNP gnomAD v4 |
X | g.154904999G>A | CA255163 | F8 | c.5398C>T (p.Arg1800Cys) c.5293C>T (p.Arg1765Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154904999G>C | CA255164 | F8 | c.5398C>G (p.Arg1800Gly) c.5293C>G (p.Arg1765Gly) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
X | g.154904999G= | CA2466828476 | F8 | c.5398C= (p.Arg1800=) c.5293C= (p.Arg1765=) | |
X | g.154904999G>T | CA414909044 | F8 | c.5398C>A (p.Arg1800Ser) c.5293C>A (p.Arg1765Ser) | |
X | g.154905002_154905003del | CA2579744567 | F8 | c.5397_5398del (p.Arg1800SerfsTer7) c.5292_5293del (p.Arg1765SerfsTer7) | |
X | g.154905000A>C | CA519357689 | F8 | c.5397T>G (p.Ser1799=) c.5292T>G (p.Ser1764=) | |
X | g.154905000A>G | CA519357690 | F8 | c.5397T>C (p.Ser1799=) c.5292T>C (p.Ser1764=) | |
X | g.154905000A>T | CA519357691 | F8 | c.5397T>A (p.Ser1799=) c.5292T>A (p.Ser1764=) | |
X | g.154905001G>A | CA414909047 | F8 | c.5396C>T (p.Ser1799Phe) c.5291C>T (p.Ser1764Phe) | |
X | g.154905001G>C | CA414909049 | F8 | c.5396C>G (p.Ser1799Cys) c.5291C>G (p.Ser1764Cys) | |
X | g.154905001G>T | CA414909051 | F8 | c.5396C>A (p.Ser1799Tyr) c.5291C>A (p.Ser1764Tyr) | |
X | g.154905002A>C | CA414909054 | F8 | c.5395T>G (p.Ser1799Ala) c.5290T>G (p.Ser1764Ala) | |
X | g.154905002A>G | CA414909056 | F8 | c.5395T>C (p.Ser1799Pro) c.5290T>C (p.Ser1764Pro) | gnomAD v4 |
X | g.154905002A>T | CA414909059 | F8 | c.5395T>A (p.Ser1799Thr) c.5290T>A (p.Ser1764Thr) | |
X | g.154905003G>A | CA519357692 | F8 | c.5394C>T (p.Ala1798=) c.5289C>T (p.Ala1763=) | gnomAD v4 |
X | g.154905003G>C | CA519357694 | F8 | c.5394C>G (p.Ala1798=) c.5289C>G (p.Ala1763=) | |
X | g.154905003G>T | CA519357693 | F8 | c.5394C>A (p.Ala1798=) c.5289C>A (p.Ala1763=) | |
X | g.154905004G>A | CA414909063 | F8 | c.5393C>T (p.Ala1798Val) c.5288C>T (p.Ala1763Val) | |
X | g.154905004G>C | CA414909067 | F8 | c.5393C>G (p.Ala1798Gly) c.5288C>G (p.Ala1763Gly) | |
X | g.154905004G= | CA2466828477 | F8 | c.5393C= (p.Ala1798=) c.5288C= (p.Ala1763=) | |
X | g.154905004G>T | CA414909064 | F8 | c.5393C>A (p.Ala1798Asp) c.5288C>A (p.Ala1763Asp) | |
X | g.154905005C>A | CA414909071 | F8 | c.5392G>T (p.Ala1798Ser) c.5287G>T (p.Ala1763Ser) | |
X | g.154905005C= | CA2466828479 | F8 | c.5392G= (p.Ala1798=) c.5287G= (p.Ala1763=) | |
X | g.154905005C>G | CA414909074 | F8 | c.5392G>C (p.Ala1798Pro) c.5287G>C (p.Ala1763Pro) | dbSNP |
X | g.154905005C>T | CA414909076 | F8 | c.5392G>A (p.Ala1798Thr) c.5287G>A (p.Ala1763Thr) | dbSNP gnomAD v4 |
X | g.154905006dup | CA2466828478 | F8 | c.5392dup (p.Ala1798GlyfsTer10) c.5287dup (p.Ala1763GlyfsTer10) | dbSNP |
X | g.154905006C>A | CA414909080 | F8 | c.5391G>T (p.Gln1797His) c.5286G>T (p.Gln1762His) | gnomAD v4 |
X | g.154905006C>G | CA414909081 | F8 | c.5391G>C (p.Gln1797His) c.5286G>C (p.Gln1762His) | |
X | g.154905006C>T | CA519357695 | F8 | c.5391G>A (p.Gln1797=) c.5286G>A (p.Gln1762=) | |
X | g.154905007T>A | CA414909090 | F8 | c.5390A>T (p.Gln1797Leu) c.5285A>T (p.Gln1762Leu) | |
X | g.154905007T>C | CA414909092 | F8 | c.5390A>G (p.Gln1797Arg) c.5285A>G (p.Gln1762Arg) | |
X | g.154905007T>G | CA414909093 | F8 | c.5390A>C (p.Gln1797Pro) c.5285A>C (p.Gln1762Pro) | |
X | g.154905008G>A | CA414909097 | F8 | c.5389C>T (p.Gln1797Ter) c.5284C>T (p.Gln1762Ter) | |
X | g.154905008G>C | CA414909098 | F8 | c.5389C>G (p.Gln1797Glu) c.5284C>G (p.Gln1762Glu) | |
X | g.154905008G>T | CA414909099 | F8 | c.5389C>A (p.Gln1797Lys) c.5284C>A (p.Gln1762Lys) | |
X | g.154905009A>C | CA414909101 | F8 | c.5388T>G (p.Asn1796Lys) c.5283T>G (p.Asn1761Lys) | |
X | g.154905009A>G | CA519357696 | F8 | c.5388T>C (p.Asn1796=) c.5283T>C (p.Asn1761=) | COSMIC COSMIC |
X | g.154905009A>T | CA414909103 | F8 | c.5388T>A (p.Asn1796Lys) c.5283T>A (p.Asn1761Lys) | |
X | g.154905010T>A | CA414909112 | F8 | c.5387A>T (p.Asn1796Ile) c.5282A>T (p.Asn1761Ile) | |
X | g.154905010T>C | CA414909107 | F8 | c.5387A>G (p.Asn1796Ser) c.5282A>G (p.Asn1761Ser) | |
X | g.154905010T>G | CA414909110 | F8 | c.5387A>C (p.Asn1796Thr) c.5282A>C (p.Asn1761Thr) | |
X | g.154905012del | CA2695238171 | F8 | c.5387del (p.Asn1796IlefsTer?) c.5282del (p.Asn1761IlefsTer?) | |
X | g.154905011T>A | CA414909115 | F8 | c.5386A>T (p.Asn1796Tyr) c.5281A>T (p.Asn1761Tyr) | |
X | g.154905011T>C | CA414909118 | F8 | c.5386A>G (p.Asn1796Asp) c.5281A>G (p.Asn1761Asp) | dbSNP |
X | g.154905011T>G | CA414909120 | F8 | c.5386A>C (p.Asn1796His) c.5281A>C (p.Asn1761His) | |
X | g.154905011T= | CA2466828480 | F8 | c.5386A= (p.Asn1796=) c.5281A= (p.Asn1761=) | |
X | g.154905012T>A | CA414909123 | F8 | c.5385A>T (p.Arg1795Ser) c.5280A>T (p.Arg1760Ser) | |
X | g.154905012T>C | CA519357697 | F8 | c.5385A>G (p.Arg1795=) c.5280A>G (p.Arg1760=) | gnomAD v4 |
X | g.154905012T>G | CA414909126 | F8 | c.5385A>C (p.Arg1795Ser) c.5280A>C (p.Arg1760Ser) | |
X | g.154905013C>A | CA414909128 | F8 | c.5384G>T (p.Arg1795Ile) c.5279G>T (p.Arg1760Ile) | |
X | g.154905013C>G | CA414909131 | F8 | c.5384G>C (p.Arg1795Thr) c.5279G>C (p.Arg1760Thr) | |
X | g.154905013C>T | CA414909134 | F8 | c.5384G>A (p.Arg1795Lys) c.5279G>A (p.Arg1760Lys) | |
X | g.154905014T>A | CA414909139 | F8 | c.5383A>T (p.Arg1795Ter) c.5278A>T (p.Arg1760Ter) | |
X | g.154905014T>C | CA414909142 | F8 | c.5383A>G (p.Arg1795Gly) c.5278A>G (p.Arg1760Gly) | gnomAD v4 |
X | g.154905014T>G | CA519357698 | F8 | c.5383A>C (p.Arg1795=) c.5278A>C (p.Arg1760=) | |
X | g.154905015G>A | CA519357699 | F8 | c.5382C>T (p.Phe1794=) c.5277C>T (p.Phe1759=) | gnomAD v3 gnomAD v4 |
X | g.154905015G>C | CA414909143 | F8 | c.5382C>G (p.Phe1794Leu) c.5277C>G (p.Phe1759Leu) | |
X | g.154905015G= | CA2466828481 | F8 | c.5382C= (p.Phe1794=) c.5277C= (p.Phe1759=) | |
X | g.154905015G>T | CA414909144 | F8 | c.5382C>A (p.Phe1794Leu) c.5277C>A (p.Phe1759Leu) | |
X | g.154905016A= | CA2466828482 | F8 | c.5381T= (p.Phe1794=) c.5276T= (p.Phe1759=) | |
X | g.154905016A>C | CA414909148 | F8 | c.5381T>G (p.Phe1794Cys) c.5276T>G (p.Phe1759Cys) | |
X | g.154905016A>G | CA414909152 | F8 | c.5381T>C (p.Phe1794Ser) c.5276T>C (p.Phe1759Ser) | |
X | g.154905016A>T | CA10567975 | F8 | c.5381T>A (p.Phe1794Tyr) c.5276T>A (p.Phe1759Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154905016_154905018delinsTC | CA2573055179 | F8 | c.5379_5381delinsGA (p.Phe1794ThrfsTer?) c.5274_5276delinsGA (p.Phe1759ThrfsTer?) | ClinVar dbSNP |
X | g.154905018dup | CA873341388 | F8 | c.5381dup (p.Arg1795GlnfsTer13) c.5276dup (p.Arg1760GlnfsTer13) | dbSNP |
X | g.154905017_154905018del | CA2695238172 | F8 | c.5380_5381del (p.Phe1794GlnfsTer13) c.5275_5276del (p.Phe1759GlnfsTer13) | |
X | g.154905017A>C | CA414909154 | F8 | c.5380T>G (p.Phe1794Val) c.5275T>G (p.Phe1759Val) | |
X | g.154905017A>G | CA414909158 | F8 | c.5380T>C (p.Phe1794Leu) c.5275T>C (p.Phe1759Leu) | |
X | g.154905017A>T | CA414909160 | F8 | c.5380T>A (p.Phe1794Ile) c.5275T>A (p.Phe1759Ile) | |
X | g.154905018A>C | CA519357700 | F8 | c.5379T>G (p.Thr1793=) c.5274T>G (p.Thr1758=) | |
X | g.154905018A>G | CA519357701 | F8 | c.5379T>C (p.Thr1793=) c.5274T>C (p.Thr1758=) | |
X | g.154905018A>T | CA519357702 | F8 | c.5379T>A (p.Thr1793=) c.5274T>A (p.Thr1758=) | |
X | g.154905019del | CA2695238174 | F8 | c.5378del (p.Thr1793IlefsTer?) c.5273del (p.Thr1758IlefsTer?) | |
X | g.154905019G>A | CA414909163 | F8 | c.5378C>T (p.Thr1793Ile) c.5273C>T (p.Thr1758Ile) | COSMIC COSMIC |
X | g.154905019G>C | CA414909165 | F8 | c.5378C>G (p.Thr1793Ser) c.5273C>G (p.Thr1758Ser) | |
X | g.154905019G= | CA2466828483 | F8 | c.5378C= (p.Thr1793=) c.5273C= (p.Thr1758=) | |
X | g.154905019G>T | CA414909167 | F8 | c.5378C>A (p.Thr1793Asn) c.5273C>A (p.Thr1758Asn) | dbSNP gnomAD v4 |
X | g.154905020T>A | CA414909172 | F8 | c.5377A>T (p.Thr1793Ser) c.5272A>T (p.Thr1758Ser) | |
X | g.154905020T>C | CA414909175 | F8 | c.5377A>G (p.Thr1793Ala) c.5272A>G (p.Thr1758Ala) | |
X | g.154905020T>G | CA414909177 | F8 | c.5377A>C (p.Thr1793Pro) c.5272A>C (p.Thr1758Pro) | |
X | g.154905021T>A | CA519357703 | F8 | c.5376A>T (p.Val1792=) c.5271A>T (p.Val1757=) | |
X | g.154905021T>C | CA10567976 | F8 | c.5376A>G (p.Val1792=) c.5271A>G (p.Val1757=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154905021T>G | CA519357704 | F8 | c.5376A>C (p.Val1792=) c.5271A>C (p.Val1757=) | |
X | g.154905021T= | CA2466828484 | F8 | c.5376A= (p.Val1792=) c.5271A= (p.Val1757=) | |
X | g.154905022A>C | CA414909184 | F8 | c.5375T>G (p.Val1792Gly) c.5270T>G (p.Val1757Gly) | |
X | g.154905022A>G | CA414909181 | F8 | c.5375T>C (p.Val1792Ala) c.5270T>C (p.Val1757Ala) | gnomAD v4 |
X | g.154905022A>T | CA414909180 | F8 | c.5375T>A (p.Val1792Glu) c.5270T>A (p.Val1757Glu) | |
X | g.154905023C>A | CA414909187 | F8 | c.5374G>T (p.Val1792Leu) c.5269G>T (p.Val1757Leu) | |
X | g.154905023C>G | CA414909188 | F8 | c.5374G>C (p.Val1792Leu) c.5269G>C (p.Val1757Leu) | |
X | g.154905023C>T | CA414909189 | F8 | c.5374G>A (p.Val1792Ile) c.5269G>A (p.Val1757Ile) | |
X | g.154905024C>A | CA414909190 | F8 | c.5374-1G>T (n.5374-1G>T) c.5269-1G>T (n.5269-1G>T) | dbSNP gnomAD v4 |
X | g.154905024C= | CA2466828485 | F8 | c.5374-1G= (n.5374-1G=) c.5269-1G= (n.5269-1G=) | |
X | g.154905024C>G | CA414909191 | F8 | c.5374-1G>C (n.5374-1G>C) c.5269-1G>C (n.5269-1G>C) | |
X | g.154905024C>T | CA414909192 | F8 | c.5374-1G>A (n.5374-1G>A) c.5269-1G>A (n.5269-1G>A) | |
X | g.154905025T>A | CA414909194 | F8 | c.5374-2A>T (n.5374-2A>T) c.5269-2A>T (n.5269-2A>T) | |
X | g.154905025T>C | CA414909197 | F8 | c.5374-2A>G (n.5374-2A>G) c.5269-2A>G (n.5269-2A>G) | gnomAD v4 |
X | g.154905025T>G | CA414909199 | F8 | c.5374-2A>C (n.5374-2A>C) c.5269-2A>C (n.5269-2A>C) | |
X | g.154905026del | CA2695238177 | F8 | c.5374-3del (n.5374-3del) c.5269-3del (n.5269-3del) | |
X | g.154905026G>T | CA2695168148 | F8 | c.5374-3C>A (n.5374-3C>A) c.5269-3C>A (n.5269-3C>A) | gnomAD v4 |
X | g.154905027del | CA2695168149 | F8 | c.5374-4del (n.5374-4del) c.5269-4del (n.5269-4del) | gnomAD v4 |
X | g.154905027T>A | CA1138596870 | F8 | c.5374-4A>T (n.5374-4A>T) c.5269-4A>T (n.5269-4A>T) | gnomAD v3 gnomAD v4 |
X | g.154905027T>G | CA10567977 | F8 | c.5374-4A>C (n.5374-4A>C) c.5269-4A>C (n.5269-4A>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154905027T= | CA2466828486 | F8 | c.5374-4A= (n.5374-4A=) c.5269-4A= (n.5269-4A=) | |
X | g.154905028A= | CA2466828487 | F8 | c.5374-5T= (n.5374-5T=) c.5269-5T= (n.5269-5T=) | |
X | g.154905028A>G | CA10567978 | F8 | c.5374-5T>C (n.5374-5T>C) c.5269-5T>C (n.5269-5T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154905029del | CA2824314880 | F8 | c.5374-6del (n.5374-6del) c.5269-6del (n.5269-6del) | |
X | g.154905029G>A | CA645292794 | F8 | c.5374-6C>T (n.5374-6C>T) c.5269-6C>T (n.5269-6C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154905029G= | CA2466828488 | F8 | c.5374-6C= (n.5374-6C=) c.5269-6C= (n.5269-6C=) | |
X | g.154905029G>T | CA2695168150 | F8 | c.5374-6C>A (n.5374-6C>A) c.5269-6C>A (n.5269-6C>A) | gnomAD v4 |
X | g.154905031_154905032insAAAA | CA2824314881 | F8 | c.5374-7_5374-6insTTTT (n.5374-7_5374-6insTTTT) c.5269-7_5269-6insTTTT (n.5269-7_5269-6insTTTT) | |
X | g.154905031_154905032delinsAC | CA2466828489 | F8 | c.5374-9_5374-8delinsGT (n.5374-9_5374-8delinsGT) c.5269-9_5269-8delinsGT (n.5269-9_5269-8delinsGT) | |
X | g.154905032del | CA645292796 | F8 | c.5374-9del (n.5374-9del) c.5269-9del (n.5269-9del) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154905032C>A | CA645292795 | F8 | c.5374-9G>T (n.5374-9G>T) c.5269-9G>T (n.5269-9G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154905032C= | CA2466828490 | F8 | c.5374-9G= (n.5374-9G=) c.5269-9G= (n.5269-9G=) | |
X | g.154905032C>T | CA2695168151 | F8 | c.5374-9G>A (n.5374-9G>A) c.5269-9G>A (n.5269-9G>A) | gnomAD v4 |