Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.51807024C>ACA384887325SCN8Ac.5538C>A (p.Asp1846Glu)
c.5415C>A (p.Asp1805Glu)
c.5571C>A (p.Asp1857Glu)
ClinVar dbSNP
12g.51807024C=CA2036194269SCN8Ac.5538C= (p.Asp1846=)
c.5415C= (p.Asp1805=)
c.5571C= (p.Asp1857=)
12g.51807024C>GCA384887312SCN8Ac.5538C>G (p.Asp1846Glu)
c.5415C>G (p.Asp1805Glu)
c.5571C>G (p.Asp1857Glu)
12g.51807024C>TCA480061943SCN8Ac.5538C>T (p.Asp1846=)
c.5415C>T (p.Asp1805=)
c.5571C>T (p.Asp1857=)
dbSNP
12g.51807025A>CCA384887332SCN8Ac.5539A>C (p.Ile1847Leu)
c.5416A>C (p.Ile1806Leu)
c.5572A>C (p.Ile1858Leu)
12g.51807025A>GCA384887336SCN8Ac.5539A>G (p.Ile1847Val)
c.5416A>G (p.Ile1806Val)
c.5572A>G (p.Ile1858Val)
12g.51807025A>TCA384887340SCN8Ac.5539A>T (p.Ile1847Phe)
c.5416A>T (p.Ile1806Phe)
c.5572A>T (p.Ile1858Phe)
12g.51807026T>ACA384887345SCN8Ac.5540T>A (p.Ile1847Asn)
c.5417T>A (p.Ile1806Asn)
c.5573T>A (p.Ile1858Asn)
12g.51807026T>CCA384887349SCN8Ac.5540T>C (p.Ile1847Thr)
c.5417T>C (p.Ile1806Thr)
c.5573T>C (p.Ile1858Thr)
12g.51807026T>GCA384887354SCN8Ac.5540T>G (p.Ile1847Ser)
c.5417T>G (p.Ile1806Ser)
c.5573T>G (p.Ile1858Ser)
12g.51807027C>ACA480061947SCN8Ac.5541C>A (p.Ile1847=)
c.5418C>A (p.Ile1806=)
c.5574C>A (p.Ile1858=)
12g.51807027C>GCA384887357SCN8Ac.5541C>G (p.Ile1847Met)
c.5418C>G (p.Ile1806Met)
c.5574C>G (p.Ile1858Met)
12g.51807027C>TCA480061949SCN8Ac.5541C>T (p.Ile1847=)
c.5418C>T (p.Ile1806=)
c.5574C>T (p.Ile1858=)
12g.51807028C>ACA384887361SCN8Ac.5542C>A (p.Leu1848Ile)
c.5419C>A (p.Leu1807Ile)
c.5575C>A (p.Leu1859Ile)
12g.51807028C>GCA384887362SCN8Ac.5542C>G (p.Leu1848Val)
c.5419C>G (p.Leu1807Val)
c.5575C>G (p.Leu1859Val)
12g.51807028C>TCA384887363SCN8Ac.5542C>T (p.Leu1848Phe)
c.5419C>T (p.Leu1807Phe)
c.5575C>T (p.Leu1859Phe)
12g.51807029T>ACA384887369SCN8Ac.5543T>A (p.Leu1848His)
c.5420T>A (p.Leu1807His)
c.5576T>A (p.Leu1859His)
12g.51807029T>CCA384887372SCN8Ac.5543T>C (p.Leu1848Pro)
c.5420T>C (p.Leu1807Pro)
c.5576T>C (p.Leu1859Pro)
12g.51807029T>GCA384887376SCN8Ac.5543T>G (p.Leu1848Arg)
c.5420T>G (p.Leu1807Arg)
c.5576T>G (p.Leu1859Arg)
12g.51807030T>ACA480061953SCN8Ac.5544T>A (p.Leu1848=)
c.5421T>A (p.Leu1807=)
c.5577T>A (p.Leu1859=)
12g.51807030T>CCA236327674SCN8Ac.5544T>C (p.Leu1848=)
c.5421T>C (p.Leu1807=)
c.5577T>C (p.Leu1859=)
dbSNP gnomAD v4
12g.51807030T>GCA480061952SCN8Ac.5544T>G (p.Leu1848=)
c.5421T>G (p.Leu1807=)
c.5577T>G (p.Leu1859=)
12g.51807030T=CA2036194272SCN8Ac.5544T= (p.Leu1848=)
c.5421T= (p.Leu1807=)
c.5577T= (p.Leu1859=)
12g.51807031T>ACA384887385SCN8Ac.5545T>A (p.Phe1849Ile)
c.5422T>A (p.Phe1808Ile)
c.5578T>A (p.Phe1860Ile)
12g.51807031T>CCA384887389SCN8Ac.5545T>C (p.Phe1849Leu)
c.5422T>C (p.Phe1808Leu)
c.5578T>C (p.Phe1860Leu)
12g.51807031T>GCA384887382SCN8Ac.5545T>G (p.Phe1849Val)
c.5422T>G (p.Phe1808Val)
c.5578T>G (p.Phe1860Val)
12g.51807032T>ACA384887398SCN8Ac.5546T>A (p.Phe1849Tyr)
c.5423T>A (p.Phe1808Tyr)
c.5579T>A (p.Phe1860Tyr)
12g.51807032T>CCA384887394SCN8Ac.5546T>C (p.Phe1849Ser)
c.5423T>C (p.Phe1808Ser)
c.5579T>C (p.Phe1860Ser)
12g.51807032T>GCA384887399SCN8Ac.5546T>G (p.Phe1849Cys)
c.5423T>G (p.Phe1808Cys)
c.5579T>G (p.Phe1860Cys)
dbSNP gnomAD v3 gnomAD v4
12g.51807032T=CA2036194277SCN8Ac.5546T= (p.Phe1849=)
c.5423T= (p.Phe1808=)
c.5579T= (p.Phe1860=)
12g.51807033T>ACA384887400SCN8Ac.5547T>A (p.Phe1849Leu)
c.5424T>A (p.Phe1808Leu)
c.5580T>A (p.Phe1860Leu)
12g.51807033T>CCA480061957SCN8Ac.5547T>C (p.Phe1849=)
c.5424T>C (p.Phe1808=)
c.5580T>C (p.Phe1860=)
12g.51807033T>GCA384887401SCN8Ac.5547T>G (p.Phe1849Leu)
c.5424T>G (p.Phe1808Leu)
c.5580T>G (p.Phe1860Leu)
ClinVar dbSNP
12g.51807034G>ACA384887404SCN8Ac.5548G>A (p.Ala1850Thr)
c.5425G>A (p.Ala1809Thr)
c.5581G>A (p.Ala1861Thr)
12g.51807034G>CCA384887406SCN8Ac.5548G>C (p.Ala1850Pro)
c.5425G>C (p.Ala1809Pro)
c.5581G>C (p.Ala1861Pro)
12g.51807034G>TCA384887405SCN8Ac.5548G>T (p.Ala1850Ser)
c.5425G>T (p.Ala1809Ser)
c.5581G>T (p.Ala1861Ser)
12g.51807035C>ACA384887409SCN8Ac.5549C>A (p.Ala1850Asp)
c.5426C>A (p.Ala1809Asp)
c.5582C>A (p.Ala1861Asp)
12g.51807035C=CA2036194286SCN8Ac.5549C= (p.Ala1850=)
c.5426C= (p.Ala1809=)
c.5582C= (p.Ala1861=)
12g.51807035C>GCA384887417SCN8Ac.5549C>G (p.Ala1850Gly)
c.5426C>G (p.Ala1809Gly)
c.5582C>G (p.Ala1861Gly)
12g.51807035C>TCA384887413SCN8Ac.5549C>T (p.Ala1850Val)
c.5426C>T (p.Ala1809Val)
c.5582C>T (p.Ala1861Val)
ClinVar dbSNP
12g.51807036C>ACA480061960SCN8Ac.5550C>A (p.Ala1850=)
c.5427C>A (p.Ala1809=)
c.5583C>A (p.Ala1861=)
12g.51807036C>GCA480061959SCN8Ac.5550C>G (p.Ala1850=)
c.5427C>G (p.Ala1809=)
c.5583C>G (p.Ala1861=)
12g.51807036C>TCA480061961SCN8Ac.5550C>T (p.Ala1850=)
c.5427C>T (p.Ala1809=)
c.5583C>T (p.Ala1861=)
12g.51807037T>ACA384887426SCN8Ac.5551T>A (p.Phe1851Ile)
c.5428T>A (p.Phe1810Ile)
c.5584T>A (p.Phe1862Ile)
12g.51807037T>CCA384887437SCN8Ac.5551T>C (p.Phe1851Leu)
c.5428T>C (p.Phe1810Leu)
c.5584T>C (p.Phe1862Leu)
12g.51807037T>GCA384887431SCN8Ac.5551T>G (p.Phe1851Val)
c.5428T>G (p.Phe1810Val)
c.5584T>G (p.Phe1862Val)
COSMIC COSMIC
12g.51807038T>ACA384887441SCN8Ac.5552T>A (p.Phe1851Tyr)
c.5429T>A (p.Phe1810Tyr)
c.5585T>A (p.Phe1862Tyr)
12g.51807038T>CCA384887448SCN8Ac.5552T>C (p.Phe1851Ser)
c.5429T>C (p.Phe1810Ser)
c.5585T>C (p.Phe1862Ser)
12g.51807038T>GCA384887444SCN8Ac.5552T>G (p.Phe1851Cys)
c.5429T>G (p.Phe1810Cys)
c.5585T>G (p.Phe1862Cys)
12g.51807039C>ACA384887453SCN8Ac.5553C>A (p.Phe1851Leu)
c.5430C>A (p.Phe1810Leu)
c.5586C>A (p.Phe1862Leu)

Number of alleles fetched