Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38550806C>ACA352140822SCN5Ac.5563G>T (p.Ala1855Ser)
c.5566G>T (p.Ala1856Ser)
c.5512G>T (p.Ala1838Ser)
c.5404G>T (p.Ala1802Ser)
c.5467G>T (p.Ala1823Ser)
c.5437G>T (p.Ala1813Ser)
c.5509G>T (p.Ala1837Ser)
3g.38550806C>GCA352140824SCN5Ac.5563G>C (p.Ala1855Pro)
c.5566G>C (p.Ala1856Pro)
c.5512G>C (p.Ala1838Pro)
c.5404G>C (p.Ala1802Pro)
c.5467G>C (p.Ala1823Pro)
c.5437G>C (p.Ala1813Pro)
c.5509G>C (p.Ala1837Pro)
ClinVar
3g.38550806C>TCA352140826SCN5Ac.5563G>A (p.Ala1855Thr)
c.5566G>A (p.Ala1856Thr)
c.5512G>A (p.Ala1838Thr)
c.5404G>A (p.Ala1802Thr)
c.5467G>A (p.Ala1823Thr)
c.5437G>A (p.Ala1813Thr)
c.5509G>A (p.Ala1837Thr)
COSMIC COSMIC COSMIC
3g.38550807A>CCA352140828SCN5Ac.5562T>G (p.Phe1854Leu)
c.5565T>G (p.Phe1855Leu)
c.5511T>G (p.Phe1837Leu)
c.5403T>G (p.Phe1801Leu)
c.5466T>G (p.Phe1822Leu)
c.5436T>G (p.Phe1812Leu)
c.5508T>G (p.Phe1836Leu)
3g.38550807A>GCA433332057SCN5Ac.5562T>C (p.Phe1854=)
c.5565T>C (p.Phe1855=)
c.5511T>C (p.Phe1837=)
c.5403T>C (p.Phe1801=)
c.5466T>C (p.Phe1822=)
c.5436T>C (p.Phe1812=)
c.5508T>C (p.Phe1836=)
3g.38550807A>TCA352140830SCN5Ac.5562T>A (p.Phe1854Leu)
c.5565T>A (p.Phe1855Leu)
c.5511T>A (p.Phe1837Leu)
c.5403T>A (p.Phe1801Leu)
c.5466T>A (p.Phe1822Leu)
c.5436T>A (p.Phe1812Leu)
c.5508T>A (p.Phe1836Leu)
3g.38550808A>CCA352140832SCN5Ac.5561T>G (p.Phe1854Cys)
c.5564T>G (p.Phe1855Cys)
c.5510T>G (p.Phe1837Cys)
c.5402T>G (p.Phe1801Cys)
c.5465T>G (p.Phe1822Cys)
c.5435T>G (p.Phe1812Cys)
c.5507T>G (p.Phe1836Cys)
3g.38550808A>GCA352140834SCN5Ac.5561T>C (p.Phe1854Ser)
c.5564T>C (p.Phe1855Ser)
c.5510T>C (p.Phe1837Ser)
c.5402T>C (p.Phe1801Ser)
c.5465T>C (p.Phe1822Ser)
c.5435T>C (p.Phe1812Ser)
c.5507T>C (p.Phe1836Ser)
ClinVar dbSNP
3g.38550808A>TCA352140836SCN5Ac.5561T>A (p.Phe1854Tyr)
c.5564T>A (p.Phe1855Tyr)
c.5510T>A (p.Phe1837Tyr)
c.5402T>A (p.Phe1801Tyr)
c.5465T>A (p.Phe1822Tyr)
c.5435T>A (p.Phe1812Tyr)
c.5507T>A (p.Phe1836Tyr)
3g.38550809A>CCA352140837SCN5Ac.5560T>G (p.Phe1854Val)
c.5563T>G (p.Phe1855Val)
c.5509T>G (p.Phe1837Val)
c.5401T>G (p.Phe1801Val)
c.5464T>G (p.Phe1822Val)
c.5434T>G (p.Phe1812Val)
c.5506T>G (p.Phe1836Val)
3g.38550809A>GCA352140839SCN5Ac.5560T>C (p.Phe1854Leu)
c.5563T>C (p.Phe1855Leu)
c.5509T>C (p.Phe1837Leu)
c.5401T>C (p.Phe1801Leu)
c.5464T>C (p.Phe1822Leu)
c.5434T>C (p.Phe1812Leu)
c.5506T>C (p.Phe1836Leu)
3g.38550809A>TCA352140840SCN5Ac.5560T>A (p.Phe1854Ile)
c.5563T>A (p.Phe1855Ile)
c.5509T>A (p.Phe1837Ile)
c.5401T>A (p.Phe1801Ile)
c.5464T>A (p.Phe1822Ile)
c.5434T>A (p.Phe1812Ile)
c.5506T>A (p.Phe1836Ile)
3g.38550810G>ACA064545SCN5Ac.5559C>T (p.Leu1853=)
c.5562C>T (p.Leu1854=)
c.5508C>T (p.Leu1836=)
c.5400C>T (p.Leu1800=)
c.5463C>T (p.Leu1821=)
c.5433C>T (p.Leu1811=)
c.5505C>T (p.Leu1835=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38550810G>CCA433332060SCN5Ac.5559C>G (p.Leu1853=)
c.5562C>G (p.Leu1854=)
c.5508C>G (p.Leu1836=)
c.5400C>G (p.Leu1800=)
c.5463C>G (p.Leu1821=)
c.5433C>G (p.Leu1811=)
c.5505C>G (p.Leu1835=)
3g.38550810G=CA1358556638SCN5Ac.5559C= (p.Leu1853=)
c.5562C= (p.Leu1854=)
c.5508C= (p.Leu1836=)
c.5400C= (p.Leu1800=)
c.5463C= (p.Leu1821=)
c.5433C= (p.Leu1811=)
c.5505C= (p.Leu1835=)
3g.38550810G>TCA433332061SCN5Ac.5559C>A (p.Leu1853=)
c.5562C>A (p.Leu1854=)
c.5508C>A (p.Leu1836=)
c.5400C>A (p.Leu1800=)
c.5463C>A (p.Leu1821=)
c.5433C>A (p.Leu1811=)
c.5505C>A (p.Leu1835=)
3g.38550811A>CCA352140843SCN5Ac.5558T>G (p.Leu1853Arg)
c.5561T>G (p.Leu1854Arg)
c.5507T>G (p.Leu1836Arg)
c.5399T>G (p.Leu1800Arg)
c.5462T>G (p.Leu1821Arg)
c.5432T>G (p.Leu1811Arg)
c.5504T>G (p.Leu1835Arg)
3g.38550811A>GCA352140842SCN5Ac.5558T>C (p.Leu1853Pro)
c.5561T>C (p.Leu1854Pro)
c.5507T>C (p.Leu1836Pro)
c.5399T>C (p.Leu1800Pro)
c.5462T>C (p.Leu1821Pro)
c.5432T>C (p.Leu1811Pro)
c.5504T>C (p.Leu1835Pro)
3g.38550811A>TCA352140841SCN5Ac.5558T>A (p.Leu1853His)
c.5561T>A (p.Leu1854His)
c.5507T>A (p.Leu1836His)
c.5399T>A (p.Leu1800His)
c.5462T>A (p.Leu1821His)
c.5432T>A (p.Leu1811His)
c.5504T>A (p.Leu1835His)
3g.38550812G>ACA352140846SCN5Ac.5557C>T (p.Leu1853Phe)
c.5560C>T (p.Leu1854Phe)
c.5506C>T (p.Leu1836Phe)
c.5398C>T (p.Leu1800Phe)
c.5461C>T (p.Leu1821Phe)
c.5431C>T (p.Leu1811Phe)
c.5503C>T (p.Leu1835Phe)
3g.38550812G>CCA352140844SCN5Ac.5557C>G (p.Leu1853Val)
c.5560C>G (p.Leu1854Val)
c.5506C>G (p.Leu1836Val)
c.5398C>G (p.Leu1800Val)
c.5461C>G (p.Leu1821Val)
c.5431C>G (p.Leu1811Val)
c.5503C>G (p.Leu1835Val)
3g.38550812G>TCA352140845SCN5Ac.5557C>A (p.Leu1853Ile)
c.5560C>A (p.Leu1854Ile)
c.5506C>A (p.Leu1836Ile)
c.5398C>A (p.Leu1800Ile)
c.5461C>A (p.Leu1821Ile)
c.5431C>A (p.Leu1811Ile)
c.5503C>A (p.Leu1835Ile)
3g.38550813A=CA1358556643SCN5Ac.5556T= (p.Ile1852=)
c.5559T= (p.Ile1853=)
c.5505T= (p.Ile1835=)
c.5397T= (p.Ile1799=)
c.5460T= (p.Ile1820=)
c.5430T= (p.Ile1810=)
c.5502T= (p.Ile1834=)
3g.38550813A>CCA352140847SCN5Ac.5556T>G (p.Ile1852Met)
c.5559T>G (p.Ile1853Met)
c.5505T>G (p.Ile1835Met)
c.5397T>G (p.Ile1799Met)
c.5460T>G (p.Ile1820Met)
c.5430T>G (p.Ile1810Met)
c.5502T>G (p.Ile1834Met)
3g.38550813A>GCA064537SCN5Ac.5556T>C (p.Ile1852=)
c.5559T>C (p.Ile1853=)
c.5505T>C (p.Ile1835=)
c.5397T>C (p.Ile1799=)
c.5460T>C (p.Ile1820=)
c.5430T>C (p.Ile1810=)
c.5502T>C (p.Ile1834=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38550813A>TCA433332062SCN5Ac.5556T>A (p.Ile1852=)
c.5559T>A (p.Ile1853=)
c.5505T>A (p.Ile1835=)
c.5397T>A (p.Ile1799=)
c.5460T>A (p.Ile1820=)
c.5430T>A (p.Ile1810=)
c.5502T>A (p.Ile1834=)
3g.38550814A>CCA352140848SCN5Ac.5555T>G (p.Ile1852Ser)
c.5558T>G (p.Ile1853Ser)
c.5504T>G (p.Ile1835Ser)
c.5396T>G (p.Ile1799Ser)
c.5459T>G (p.Ile1820Ser)
c.5429T>G (p.Ile1810Ser)
c.5501T>G (p.Ile1834Ser)
3g.38550814A>GCA352140849SCN5Ac.5555T>C (p.Ile1852Thr)
c.5558T>C (p.Ile1853Thr)
c.5504T>C (p.Ile1835Thr)
c.5396T>C (p.Ile1799Thr)
c.5459T>C (p.Ile1820Thr)
c.5429T>C (p.Ile1810Thr)
c.5501T>C (p.Ile1834Thr)
3g.38550814A>TCA352140850SCN5Ac.5555T>A (p.Ile1852Asn)
c.5558T>A (p.Ile1853Asn)
c.5504T>A (p.Ile1835Asn)
c.5396T>A (p.Ile1799Asn)
c.5459T>A (p.Ile1820Asn)
c.5429T>A (p.Ile1810Asn)
c.5501T>A (p.Ile1834Asn)
3g.38550815T>ACA352140851SCN5Ac.5554A>T (p.Ile1852Phe)
c.5557A>T (p.Ile1853Phe)
c.5503A>T (p.Ile1835Phe)
c.5395A>T (p.Ile1799Phe)
c.5458A>T (p.Ile1820Phe)
c.5428A>T (p.Ile1810Phe)
c.5500A>T (p.Ile1834Phe)
3g.38550815T>CCA352140852SCN5Ac.5554A>G (p.Ile1852Val)
c.5557A>G (p.Ile1853Val)
c.5503A>G (p.Ile1835Val)
c.5395A>G (p.Ile1799Val)
c.5458A>G (p.Ile1820Val)
c.5428A>G (p.Ile1810Val)
c.5500A>G (p.Ile1834Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38550815T>GCA352140853SCN5Ac.5554A>C (p.Ile1852Leu)
c.5557A>C (p.Ile1853Leu)
c.5503A>C (p.Ile1835Leu)
c.5395A>C (p.Ile1799Leu)
c.5458A>C (p.Ile1820Leu)
c.5428A>C (p.Ile1810Leu)
c.5500A>C (p.Ile1834Leu)
ClinVar dbSNP
3g.38550815T=CA1358556649SCN5Ac.5554A= (p.Ile1852=)
c.5557A= (p.Ile1853=)
c.5503A= (p.Ile1835=)
c.5395A= (p.Ile1799=)
c.5458A= (p.Ile1820=)
c.5428A= (p.Ile1810=)
c.5500A= (p.Ile1834=)
3g.38550816G>ACA433332064SCN5Ac.5553C>T (p.Asp1851=)
c.5556C>T (p.Asp1852=)
c.5502C>T (p.Asp1834=)
c.5394C>T (p.Asp1798=)
c.5457C>T (p.Asp1819=)
c.5427C>T (p.Asp1809=)
c.5499C>T (p.Asp1833=)
ClinVar dbSNP gnomAD v2
3g.38550816G>CCA352140854SCN5Ac.5553C>G (p.Asp1851Glu)
c.5556C>G (p.Asp1852Glu)
c.5502C>G (p.Asp1834Glu)
c.5394C>G (p.Asp1798Glu)
c.5457C>G (p.Asp1819Glu)
c.5427C>G (p.Asp1809Glu)
c.5499C>G (p.Asp1833Glu)
3g.38550816G=CA1358556655SCN5Ac.5553C= (p.Asp1851=)
c.5556C= (p.Asp1852=)
c.5502C= (p.Asp1834=)
c.5394C= (p.Asp1798=)
c.5457C= (p.Asp1819=)
c.5427C= (p.Asp1809=)
c.5499C= (p.Asp1833=)
3g.38550816G>TCA352140855SCN5Ac.5553C>A (p.Asp1851Glu)
c.5556C>A (p.Asp1852Glu)
c.5502C>A (p.Asp1834Glu)
c.5394C>A (p.Asp1798Glu)
c.5457C>A (p.Asp1819Glu)
c.5427C>A (p.Asp1809Glu)
c.5499C>A (p.Asp1833Glu)
3g.38550817T>ACA064529SCN5Ac.5552A>T (p.Asp1851Val)
c.5555A>T (p.Asp1852Val)
c.5501A>T (p.Asp1834Val)
c.5393A>T (p.Asp1798Val)
c.5456A>T (p.Asp1819Val)
c.5426A>T (p.Asp1809Val)
c.5498A>T (p.Asp1833Val)
ClinVar dbSNP ExAC gnomAD v2
3g.38550817T>CCA352140857SCN5Ac.5552A>G (p.Asp1851Gly)
c.5555A>G (p.Asp1852Gly)
c.5501A>G (p.Asp1834Gly)
c.5393A>G (p.Asp1798Gly)
c.5456A>G (p.Asp1819Gly)
c.5426A>G (p.Asp1809Gly)
c.5498A>G (p.Asp1833Gly)
3g.38550817T>GCA352140856SCN5Ac.5552A>C (p.Asp1851Ala)
c.5555A>C (p.Asp1852Ala)
c.5501A>C (p.Asp1834Ala)
c.5393A>C (p.Asp1798Ala)
c.5456A>C (p.Asp1819Ala)
c.5426A>C (p.Asp1809Ala)
c.5498A>C (p.Asp1833Ala)
3g.38550817T=CA1358556659SCN5Ac.5552A= (p.Asp1851=)
c.5555A= (p.Asp1852=)
c.5501A= (p.Asp1834=)
c.5393A= (p.Asp1798=)
c.5456A= (p.Asp1819=)
c.5426A= (p.Asp1809=)
c.5498A= (p.Asp1833=)
3g.38550818C>ACA352140858SCN5Ac.5551G>T (p.Asp1851Tyr)
c.5554G>T (p.Asp1852Tyr)
c.5500G>T (p.Asp1834Tyr)
c.5392G>T (p.Asp1798Tyr)
c.5455G>T (p.Asp1819Tyr)
c.5425G>T (p.Asp1809Tyr)
c.5497G>T (p.Asp1833Tyr)
3g.38550818C>GCA352140859SCN5Ac.5551G>C (p.Asp1851His)
c.5554G>C (p.Asp1852His)
c.5500G>C (p.Asp1834His)
c.5392G>C (p.Asp1798His)
c.5455G>C (p.Asp1819His)
c.5425G>C (p.Asp1809His)
c.5497G>C (p.Asp1833His)
3g.38550818C>TCA352140860SCN5Ac.5551G>A (p.Asp1851Asn)
c.5554G>A (p.Asp1852Asn)
c.5500G>A (p.Asp1834Asn)
c.5392G>A (p.Asp1798Asn)
c.5455G>A (p.Asp1819Asn)
c.5425G>A (p.Asp1809Asn)
c.5497G>A (p.Asp1833Asn)
gnomAD v4
3g.38550819C>ACA352140861SCN5Ac.5550G>T (p.Met1850Ile)
c.5553G>T (p.Met1851Ile)
c.5499G>T (p.Met1833Ile)
c.5391G>T (p.Met1797Ile)
c.5454G>T (p.Met1818Ile)
c.5424G>T (p.Met1808Ile)
c.5496G>T (p.Met1832Ile)
3g.38550819C=CA1358556662SCN5Ac.5550G= (p.Met1850=)
c.5553G= (p.Met1851=)
c.5499G= (p.Met1833=)
c.5391G= (p.Met1797=)
c.5454G= (p.Met1818=)
c.5424G= (p.Met1808=)
c.5496G= (p.Met1832=)
3g.38550819C>GCA352140862SCN5Ac.5550G>C (p.Met1850Ile)
c.5553G>C (p.Met1851Ile)
c.5499G>C (p.Met1833Ile)
c.5391G>C (p.Met1797Ile)
c.5454G>C (p.Met1818Ile)
c.5424G>C (p.Met1808Ile)
c.5496G>C (p.Met1832Ile)
3g.38550819C>TCA352140863SCN5Ac.5550G>A (p.Met1850Ile)
c.5553G>A (p.Met1851Ile)
c.5499G>A (p.Met1833Ile)
c.5391G>A (p.Met1797Ile)
c.5454G>A (p.Met1818Ile)
c.5424G>A (p.Met1808Ile)
c.5496G>A (p.Met1832Ile)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38550820A=CA1358556669SCN5Ac.5549T= (p.Met1850=)
c.5552T= (p.Met1851=)
c.5498T= (p.Met1833=)
c.5390T= (p.Met1797=)
c.5453T= (p.Met1818=)
c.5423T= (p.Met1808=)
c.5495T= (p.Met1832=)
3g.38550820A>CCA352140864SCN5Ac.5549T>G (p.Met1850Arg)
c.5552T>G (p.Met1851Arg)
c.5498T>G (p.Met1833Arg)
c.5390T>G (p.Met1797Arg)
c.5453T>G (p.Met1818Arg)
c.5423T>G (p.Met1808Arg)
c.5495T>G (p.Met1832Arg)

Number of alleles fetched