Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.19954230G>ACA370468484LPLc.652G>A (p.Gly218Ser)
8g.19954230G>CCA370468483LPLc.652G>C (p.Gly218Arg)
gnomAD v4
8g.19954230G>TCA370468482LPLc.652G>T (p.Gly218Cys)
8g.19954231G>ACA4655487LPLc.653G>A (p.Gly218Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.19954231G>CCA370468486LPLc.653G>C (p.Gly218Ala)
gnomAD v4
8g.19954231G=CA1769102586LPLc.653G= (p.Gly218=)
8g.19954231G>TCA370468485LPLc.653G>T (p.Gly218Val)
8g.19954232T>ACA459879470LPLc.654T>A (p.Gly218=)
8g.19954232T>CCA459879471LPLc.654T>C (p.Gly218=)
8g.19954232T>GCA459879472LPLc.654T>G (p.Gly218=)
8g.19954233C>ACA459879473LPLc.655C>A (p.Arg219=)
dbSNP gnomAD v2 gnomAD v4
8g.19954233C=CA1769102590LPLc.655C= (p.Arg219=)
8g.19954233C>GCA370468487LPLc.655C>G (p.Arg219Gly)
gnomAD v4
8g.19954233C>TCA370468488LPLc.655C>T (p.Arg219Ter)
dbSNP gnomAD v4
8g.19954234G>ACA173377502LPLc.656G>A (p.Arg219Gln)
dbSNP gnomAD v2 gnomAD v4
8g.19954234G>CCA370468489LPLc.656G>C (p.Arg219Pro)
8g.19954234G=CA1769102596LPLc.656G= (p.Arg219=)
8g.19954234G>TCA370468490LPLc.656G>T (p.Arg219Leu)
8g.19954235A>CCA459879474LPLc.657A>C (p.Arg219=)
8g.19954235A>GCA459879475LPLc.657A>G (p.Arg219=)
8g.19954235A>TCA459879476LPLc.657A>T (p.Arg219=)
8g.19954236A=CA1769102597LPLc.658A= (p.Ser220=)
8g.19954236A>CCA4655488LPLc.658A>C (p.Ser220Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.19954236A>GCA370468491LPLc.658A>G (p.Ser220Gly)
8g.19954236A>TCA370468492LPLc.658A>T (p.Ser220Cys)
8g.19954236_19954240delinsCGCACCA2695208932LPLc.658_662delinsCGCAC (p.Ser220_Ile221delinsArgThr)
8g.19954237G>ACA370468493LPLc.659G>A (p.Ser220Asn)
ClinVar dbSNP
8g.19954237G>CCA370468494LPLc.659G>C (p.Ser220Thr)
8g.19954237G>TCA370468495LPLc.659G>T (p.Ser220Ile)
8g.19954238C>ACA370468496LPLc.660C>A (p.Ser220Arg)
8g.19954238C=CA1769102602LPLc.660C= (p.Ser220=)
8g.19954238C>GCA370468497LPLc.660C>G (p.Ser220Arg)
gnomAD v4
8g.19954238C>TCA459879477LPLc.660C>T (p.Ser220=)
dbSNP
8g.19954239A>CCA370468498LPLc.661A>C (p.Ile221Leu)
8g.19954239A>GCA370468500LPLc.661A>G (p.Ile221Val)
8g.19954239A>TCA370468499LPLc.661A>T (p.Ile221Phe)
ClinVar dbSNP
8g.19954240T>ACA370468501LPLc.662T>A (p.Ile221Asn)
ClinVar gnomAD v4 COSMIC
8g.19954240T>CCA251867LPLc.662T>C (p.Ile221Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.19954240T>GCA370468502LPLc.662T>G (p.Ile221Ser)
8g.19954240T=CA1769102614LPLc.662T= (p.Ile221=)
8g.19954241T>ACA459879478LPLc.663T>A (p.Ile221=)
8g.19954241T>CCA459879479LPLc.663T>C (p.Ile221=)
8g.19954241T>GCA370468503LPLc.663T>G (p.Ile221Met)
8g.19954242G>ACA370468504LPLc.664G>A (p.Gly222Arg)
8g.19954242G>CCA370468505LPLc.664G>C (p.Gly222Arg)
8g.19954242G>TCA370468506LPLc.664G>T (p.Gly222Ter)
8g.19954243G>ACA251884LPLc.665G>A (p.Gly222Glu)
ClinVar dbSNP
8g.19954243G>CCA370468507LPLc.665G>C (p.Gly222Ala)
8g.19954243G=CA1769102620LPLc.665G= (p.Gly222=)
8g.19954243G>TCA370468508LPLc.665G>T (p.Gly222Val)

Number of alleles fetched