Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.19966981T>ACA849568013LPLc.*1671T>A (p.=)
n.2039T>A (p.=)
8g.19966981T>CCA130748LPLc.*1671T>C (p.=)
n.2039T>C (p.=)
ClinVar dbSNP gnomAD
8g.19966981T=CA1769116695LPLc.*1671T= (p.=)
n.2039T= (p.=)
8g.19966982T>CCA1111558914LPLc.*1672T>C (p.=)
n.2040T>C (p.=)
8g.19966982T=CA1769116701LPLc.*1672T= (p.=)
n.2040T= (p.=)
8g.19966989_19966990dupCA1111558911LPLc.*1679_*1680dup (p.=)
n.2047_2048dup (p.=)
dbSNP
8g.19966983A=CA1769116705LPLc.*1673A= (p.=)
n.2041A= (p.=)
8g.19966983A>GCA1769116703LPLc.*1673A>G (p.=)
n.2041A>G (p.=)
8g.19966986T>CCA173618758LPLc.*1676T>C (p.=)
n.2044T>C (p.=)
dbSNP gnomAD
8g.19966986T=CA1769116707LPLc.*1676T= (p.=)
n.2044T= (p.=)
8g.19966998G>CCA580209973LPLc.*1688G>C (p.=)
n.2056G>C (p.=)
gnomAD
8g.19966998G=CA1769116711LPLc.*1688G= (p.=)
n.2056G= (p.=)
8g.19967000T>CCA173618759LPLc.*1690T>C (p.=)
n.2058T>C (p.=)
dbSNP gnomAD
8g.19967000T=CA1769116713LPLc.*1690T= (p.=)
n.2058T= (p.=)
8g.19967003G=CA1769116717LPLc.*1693G= (p.=)
n.2061G= (p.=)
8g.19967003G>TCA849568017LPLc.*1693G>T (p.=)
n.2061G>T (p.=)
8g.19967004G=CA1769116718LPLc.*1694G= (p.=)
n.2062G= (p.=)
8g.19967004G>TCA580209975LPLc.*1694G>T (p.=)
n.2062G>T (p.=)
gnomAD
8g.19967005C=CA1769116720LPLc.*1695C= (p.=)
n.2063C= (p.=)
8g.19967005C>GCA580209976LPLc.*1695C>G (p.=)
n.2063C>G (p.=)
gnomAD
8g.19967005C>TCA849568024LPLc.*1695C>T (p.=)
n.2063C>T (p.=)
8g.19967006T>GCA1769116724LPLc.*1696T>G (p.=)
n.2064T>G (p.=)
8g.19967006T=CA1769116722LPLc.*1696T= (p.=)
n.2064T= (p.=)
8g.19967010C>ACA1769116726LPLc.*1700C>A (p.=)
n.2068C>A (p.=)
8g.19967010C=CA1769116725LPLc.*1700C= (p.=)
n.2068C= (p.=)
8g.19967012T>CCA1769116728LPLc.*1702T>C (p.=)
n.2070T>C (p.=)
8g.19967012T=CA1769116727LPLc.*1702T= (p.=)
n.2070T= (p.=)
8g.19967013T>CCA580209977LPLc.*1703T>C (p.=)
n.2071T>C (p.=)
gnomAD
8g.19967013T=CA1769116729LPLc.*1703T= (p.=)
n.2071T= (p.=)
8g.19967016A=CA1769116732LPLc.*1706A= (p.=)
n.2074A= (p.=)
8g.19967016A>CCA849568034LPLc.*1706A>C (p.=)
n.2074A>C (p.=)
8g.19967021_19967031delinsTTAGCTGTAAACA1769116734LPLc.*1711_*1721delinsTTAGCTGTAAA (p.=)
n.2079_2089delinsTTAGCTGTAAA (p.=)
8g.19967024_19967033delCA1111558925LPLc.*1714_*1723del (p.=)
n.2082_2091del (p.=)
dbSNP
8g.19967027G>ACA849568036LPLc.*1717G>A (p.=)
n.2085G>A (p.=)
8g.19967027G=CA1769116737LPLc.*1717G= (p.=)
n.2085G= (p.=)
8g.19967028T>CCA1111558927LPLc.*1718T>C (p.=)
n.2086T>C (p.=)
8g.19967028T=CA1769116739LPLc.*1718T= (p.=)
n.2086T= (p.=)
8g.19967032T>CCA173618760LPLc.*1722T>C (p.=)
n.2090T>C (p.=)
dbSNP
8g.19967032T=CA1769116742LPLc.*1722T= (p.=)
n.2090T= (p.=)
8g.19967034C=CA1769116745LPLc.*1724C= (p.=)
n.2092C= (p.=)
8g.19967034C>TCA849568042LPLc.*1724C>T (p.=)
n.2092C>T (p.=)
8g.19967035A=CA1769116747LPLc.*1725A= (p.=)
n.2093A= (p.=)
8g.19967035A>CCA1769116748LPLc.*1725A>C (p.=)
n.2093A>C (p.=)
8g.19967036T>CCA849568047LPLc.*1726T>C (p.=)
n.2094T>C (p.=)
8g.19967036T=CA1769116750LPLc.*1726T= (p.=)
n.2094T= (p.=)
8g.19967043A=CA1769116752LPLc.*1733A= (p.=)
n.2101A= (p.=)
8g.19967043A>GCA849568049LPLc.*1733A>G (p.=)
n.2101A>G (p.=)
8g.19967045G>ACA1769116755LPLc.*1735G>A (p.=)
n.2103G>A (p.=)
8g.19967045G=CA1769116754LPLc.*1735G= (p.=)
n.2103G= (p.=)
8g.19967048T>GCA849568050LPLc.*1738T>G (p.=)
n.2106T>G (p.=)

Number of alleles fetched