Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.204166246_204166249delinsGAGCCA2482059825RENc.45_48delinsGCTC (p.Leu15=)
c.-16-4086_-16-4083delinsGCTC (n.-16-4086_-16-4083delinsGCTC)
1g.204166247A=CA1141581511RENc.47T= (p.Leu16=)
c.-16-4084T= (n.-16-4084T=)
1g.204166247A>CCA256731RENc.47T>G (p.Leu16Arg)
c.-16-4084T>G (n.-16-4084T>G)
ClinVar dbSNP
1g.204166247A>GCA344343035RENc.47T>C (p.Leu16Pro)
c.-16-4084T>C (n.-16-4084T>C)
1g.204166247A>TCA344343036RENc.47T>A (p.Leu16His)
c.-16-4084T>A (n.-16-4084T>A)
ClinVar dbSNP
1g.204166258_204166260dupCA1011402350RENc.45_47dup (p.Leu16_Trp17insLeu)
c.-16-4086_-16-4084dup (n.-16-4086_-16-4084dup)
dbSNP gnomAD v3 gnomAD v4
1g.204166258_204166260delCA645539485RENc.45_47del (p.Leu16del)
c.-16-4086_-16-4084del (n.-16-4086_-16-4084del)
ClinVar dbSNP gnomAD v4 COSMIC
1g.204166248G>ACA344343039RENc.46C>T (p.Leu16Phe)
c.-16-4085C>T (n.-16-4085C>T)
gnomAD v4
1g.204166248G>CCA344343038RENc.46C>G (p.Leu16Val)
c.-16-4085C>G (n.-16-4085C>G)
1g.204166248G>TCA344343037RENc.46C>A (p.Leu16Ile)
c.-16-4085C>A (n.-16-4085C>A)
1g.204166249C>ACA422840545RENc.45G>T (p.Leu15=)
c.-16-4086G>T (n.-16-4086G>T)
1g.204166249C=CA1141886092RENc.45G= (p.Leu15=)
c.-16-4086G= (n.-16-4086G=)
1g.204166249C>GCA422840542RENc.45G>C (p.Leu15=)
c.-16-4086G>C (n.-16-4086G>C)
1g.204166249C>TCA1345084RENc.45G>A (p.Leu15=)
c.-16-4086G>A (n.-16-4086G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.204166250A>CCA344343042RENc.44T>G (p.Leu15Arg)
c.-16-4087T>G (n.-16-4087T>G)
1g.204166250A>GCA344343040RENc.44T>C (p.Leu15Pro)
c.-16-4087T>C (n.-16-4087T>C)
1g.204166250A>TCA344343041RENc.44T>A (p.Leu15Gln)
c.-16-4087T>A (n.-16-4087T>A)
1g.204166251G>ACA422840551RENc.43C>T (p.Leu15=)
c.-16-4088C>T (n.-16-4088C>T)
gnomAD v4
1g.204166251G>CCA344343043RENc.43C>G (p.Leu15Val)
c.-16-4088C>G (n.-16-4088C>G)
1g.204166251G>TCA344343044RENc.43C>A (p.Leu15Met)
c.-16-4088C>A (n.-16-4088C>A)
1g.204166252C>ACA422840554RENc.42G>T (p.Leu14=)
c.-16-4089G>T (n.-16-4089G>T)
1g.204166252C=CA2482059826RENc.42G= (p.Leu14=)
c.-16-4089G= (n.-16-4089G=)
1g.204166252C>GCA422840555RENc.42G>C (p.Leu14=)
c.-16-4089G>C (n.-16-4089G>C)
1g.204166252C>TCA422840557RENc.42G>A (p.Leu14=)
c.-16-4089G>A (n.-16-4089G>A)
dbSNP gnomAD v3 gnomAD v4
1g.204166253A>CCA344343045RENc.41T>G (p.Leu14Arg)
c.-16-4090T>G (n.-16-4090T>G)
1g.204166253A>GCA344343046RENc.41T>C (p.Leu14Pro)
c.-16-4090T>C (n.-16-4090T>C)
1g.204166253A>TCA344343047RENc.41T>A (p.Leu14Gln)
c.-16-4090T>A (n.-16-4090T>A)
1g.204166254G>ACA422840563RENc.40C>T (p.Leu14=)
c.-16-4091C>T (n.-16-4091C>T)
1g.204166254G>CCA344343048RENc.40C>G (p.Leu14Val)
c.-16-4091C>G (n.-16-4091C>G)
1g.204166254G>TCA344343049RENc.40C>A (p.Leu14Met)
c.-16-4091C>A (n.-16-4091C>A)
1g.204166255C>ACA422840567RENc.39G>T (p.Leu13=)
c.-16-4092G>T (n.-16-4092G>T)
1g.204166255C>GCA422840569RENc.39G>C (p.Leu13=)
c.-16-4092G>C (n.-16-4092G>C)
1g.204166255C>TCA422840570RENc.39G>A (p.Leu13=)
c.-16-4092G>A (n.-16-4092G>A)
1g.204166256A>CCA344343050RENc.38T>G (p.Leu13Arg)
c.-16-4093T>G (n.-16-4093T>G)
1g.204166256A>GCA344343051RENc.38T>C (p.Leu13Pro)
c.-16-4093T>C (n.-16-4093T>C)
1g.204166256A>TCA344343052RENc.38T>A (p.Leu13Gln)
c.-16-4093T>A (n.-16-4093T>A)
1g.204166257G>ACA422840577RENc.37C>T (p.Leu13=)
c.-16-4094C>T (n.-16-4094C>T)
1g.204166257G>CCA344343053RENc.37C>G (p.Leu13Val)
c.-16-4094C>G (n.-16-4094C>G)
1g.204166257G>TCA344343054RENc.37C>A (p.Leu13Met)
c.-16-4094C>A (n.-16-4094C>A)
1g.204166258C>ACA422840582RENc.36G>T (p.Leu12=)
c.-16-4095G>T (n.-16-4095G>T)
dbSNP
1g.204166258C=CA2482059827RENc.36G= (p.Leu12=)
c.-16-4095G= (n.-16-4095G=)
1g.204166258C>GCA422840583RENc.36G>C (p.Leu12=)
c.-16-4095G>C (n.-16-4095G>C)
1g.204166258C>TCA422840581RENc.36G>A (p.Leu12=)
c.-16-4095G>A (n.-16-4095G>A)
1g.204166259A>CCA344343057RENc.35T>G (p.Leu12Arg)
c.-16-4096T>G (n.-16-4096T>G)
1g.204166259A>GCA344343055RENc.35T>C (p.Leu12Pro)
c.-16-4096T>C (n.-16-4096T>C)
1g.204166259A>TCA344343056RENc.35T>A (p.Leu12Gln)
c.-16-4096T>A (n.-16-4096T>A)
1g.204166260G>ACA422840584RENc.34C>T (p.Leu12=)
c.-16-4097C>T (n.-16-4097C>T)
1g.204166260G>CCA344343058RENc.34C>G (p.Leu12Val)
c.-16-4097C>G (n.-16-4097C>G)
1g.204166260G=CA2482059828RENc.34C= (p.Leu12=)
c.-16-4097C= (n.-16-4097C=)
1g.204166260G>TCA344343059RENc.34C>A (p.Leu12Met)
c.-16-4097C>A (n.-16-4097C>A)
dbSNP gnomAD v2 gnomAD v4 COSMIC

Number of alleles fetched