Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.19955894G>ACA251877LPLc.829G>A (p.Asp277Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.19955894G>CCA370469041LPLc.829G>C (p.Asp277His)
8g.19955894G=CA1769104562LPLc.829G= (p.Asp277=)
8g.19955894G>TCA370469042LPLc.829G>T (p.Asp277Tyr)
gnomAD v4
8g.19955895A=CA1769104566LPLc.830A= (p.Asp277=)
8g.19955895A>CCA370469043LPLc.830A>C (p.Asp277Ala)
8g.19955895A>GCA370469044LPLc.830A>G (p.Asp277Gly)
dbSNP gnomAD v3 gnomAD v4
8g.19955895A>TCA370469045LPLc.830A>T (p.Asp277Val)
8g.19955895_19955897delinsACTCA1769104565LPLc.830_832delinsACT (p.Asp277=)
8g.19955896C>ACA370469046LPLc.831C>A (p.Asp277Glu)
8g.19955896C>GCA370469047LPLc.831C>G (p.Asp277Glu)
8g.19955896C>TCA459879444LPLc.831C>T (p.Asp277=)
ClinVar dbSNP
8g.19955900_19955901delCA4655545LPLc.835_836del (p.Leu279ValfsTer3)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.19955897T>ACA370469048LPLc.832T>A (p.Ser278Thr)
8g.19955897T>CCA370469050LPLc.832T>C (p.Ser278Pro)
8g.19955897T>GCA370469049LPLc.832T>G (p.Ser278Ala)
8g.19955898C>ACA370469051LPLc.833C>A (p.Ser278Tyr)
8g.19955898C>GCA370469052LPLc.833C>G (p.Ser278Cys)
8g.19955898C>TCA370469053LPLc.833C>T (p.Ser278Phe)
8g.19955899T>ACA459879448LPLc.834T>A (p.Ser278=)
ClinVar
8g.19955899T>CCA459879449LPLc.834T>C (p.Ser278=)
ClinVar dbSNP gnomAD v2 gnomAD v4
8g.19955899T>GCA459879450LPLc.834T>G (p.Ser278=)
8g.19955899T=CA1769104571LPLc.834T= (p.Ser278=)
8g.19955900C>ACA370469054LPLc.835C>A (p.Leu279Met)
8g.19955900C=CA1769104575LPLc.835C= (p.Leu279=)
8g.19955900C>GCA4655546LPLc.835C>G (p.Leu279Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.19955900C>TCA459879561LPLc.835C>T (p.Leu279=)
8g.19955901T>ACA370469055LPLc.836T>A (p.Leu279Gln)
gnomAD v4
8g.19955901T>CCA370469056LPLc.836T>C (p.Leu279Pro)
8g.19955901T>GCA173378278LPLc.836T>G (p.Leu279Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.19955901T=CA1769104584LPLc.836T= (p.Leu279=)
8g.19955902G>ACA459879562LPLc.837G>A (p.Leu279=)
8g.19955902G>CCA459879563LPLc.837G>C (p.Leu279=)
8g.19955902G=CA1769104591LPLc.837G= (p.Leu279=)
8g.19955902G>TCA459879564LPLc.837G>T (p.Leu279=)
dbSNP
8g.19955903T>ACA370469057LPLc.838T>A (p.Leu280Met)
8g.19955903T>CCA459879565LPLc.838T>C (p.Leu280=)
ClinVar dbSNP gnomAD v4
8g.19955903T>GCA370469058LPLc.838T>G (p.Leu280Val)
8g.19955903T=CA1769104595LPLc.838T= (p.Leu280=)
8g.19955904T>ACA370469059LPLc.839T>A (p.Leu280Ter)
8g.19955904T>CCA370469060LPLc.839T>C (p.Leu280Ser)
8g.19955904T>GCA370469061LPLc.839T>G (p.Leu280Trp)
8g.19955905delCA2695208933LPLc.840del (p.Asn281MetfsTer23)
8g.19955905G>ACA459879566LPLc.840G>A (p.Leu280=)
8g.19955905G>CCA370469062LPLc.840G>C (p.Leu280Phe)
8g.19955905G>TCA370469063LPLc.840G>T (p.Leu280Phe)
8g.19955906A>CCA370469064LPLc.841A>C (p.Asn281His)
8g.19955906A>GCA370469065LPLc.841A>G (p.Asn281Asp)
8g.19955906A>TCA370469066LPLc.841A>T (p.Asn281Tyr)
8g.19955907A=CA1769104599LPLc.842A= (p.Asn281=)

Number of alleles fetched