Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.76347130T>ACA481011420BBS10c.855A>T (p.Thr285=)
ClinVar dbSNP gnomAD v3 gnomAD v4
12g.76347130T>CCA481011422BBS10c.855A>G (p.Thr285=)
12g.76347130T>GCA481011423BBS10c.855A>C (p.Thr285=)
12g.76347130T=CA2047353633BBS10c.855A= (p.Thr285=)
12g.76347131G>ACA385813895BBS10c.854C>T (p.Thr285Ile)
gnomAD v4
12g.76347131G>CCA385813896BBS10c.854C>G (p.Thr285Arg)
12g.76347131G>TCA385813897BBS10c.854C>A (p.Thr285Lys)
12g.76347132T>ACA385813898BBS10c.853A>T (p.Thr285Ser)
12g.76347132T>CCA385813899BBS10c.853A>G (p.Thr285Ala)
12g.76347132T>GCA385813900BBS10c.853A>C (p.Thr285Pro)
12g.76347133C>ACA385813902BBS10c.852G>T (p.Gln284His)
gnomAD v4
12g.76347133C=CA2047353634BBS10c.852G= (p.Gln284=)
12g.76347133C>GCA385813901BBS10c.852G>C (p.Gln284His)
COSMIC
12g.76347133C>TCA481011430BBS10c.852G>A (p.Gln284=)
dbSNP
12g.76347134T>ACA385813903BBS10c.851A>T (p.Gln284Leu)
12g.76347134T>CCA6694274BBS10c.851A>G (p.Gln284Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.76347134T>GCA385813904BBS10c.851A>C (p.Gln284Pro)
12g.76347134T=CA2047353635BBS10c.851A= (p.Gln284=)
12g.76347135G>ACA6694275BBS10c.850C>T (p.Gln284Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.76347135G>CCA385813905BBS10c.850C>G (p.Gln284Glu)
12g.76347135G=CA2047353636BBS10c.850C= (p.Gln284=)
12g.76347135G>TCA385813906BBS10c.850C>A (p.Gln284Lys)
gnomAD v4
12g.76347136A>CCA385813907BBS10c.849T>G (p.Phe283Leu)
12g.76347136A>GCA481011438BBS10c.849T>C (p.Phe283=)
12g.76347136A>TCA385813908BBS10c.849T>A (p.Phe283Leu)
12g.76347137A>CCA385813909BBS10c.848T>G (p.Phe283Cys)
12g.76347137A>GCA385813910BBS10c.848T>C (p.Phe283Ser)
12g.76347137A>TCA385813911BBS10c.848T>A (p.Phe283Tyr)
12g.76347138A>CCA385813912BBS10c.847T>G (p.Phe283Val)
12g.76347138A>GCA385813913BBS10c.847T>C (p.Phe283Leu)
gnomAD v4
12g.76347138A>TCA385813914BBS10c.847T>A (p.Phe283Ile)
12g.76347139C>ACA385813915BBS10c.846G>T (p.Gln282His)
12g.76347139C=CA2047353637BBS10c.846G= (p.Gln282=)
12g.76347139C>GCA385813916BBS10c.846G>C (p.Gln282His)
12g.76347139C>TCA481011445BBS10c.846G>A (p.Gln282=)
dbSNP
12g.76347140T>ACA385813917BBS10c.845A>T (p.Gln282Leu)
12g.76347140T>CCA385813919BBS10c.845A>G (p.Gln282Arg)
12g.76347140T>GCA385813918BBS10c.845A>C (p.Gln282Pro)
12g.76347142_76347143delCA2575230731BBS10c.844_845del (p.Gln282ValfsTer21)
ClinVar gnomAD v4
12g.76347141G>ACA385813920BBS10c.844C>T (p.Gln282Ter)
12g.76347141G>CCA385813921BBS10c.844C>G (p.Gln282Glu)
12g.76347141G>TCA385813922BBS10c.844C>A (p.Gln282Lys)
gnomAD v4
12g.76347142T>ACA481011449BBS10c.843A>T (p.Ala281=)
12g.76347142T>CCA481011450BBS10c.843A>G (p.Ala281=)
12g.76347142T>GCA481011451BBS10c.843A>C (p.Ala281=)
ClinVar
12g.76347143G>ACA385813923BBS10c.842C>T (p.Ala281Val)
12g.76347143G>CCA385813924BBS10c.842C>G (p.Ala281Gly)
12g.76347143G>TCA385813925BBS10c.842C>A (p.Ala281Glu)
12g.76347144C>ACA385813926BBS10c.841G>T (p.Ala281Ser)
12g.76347144C=CA2047353638BBS10c.841G= (p.Ala281=)

Number of alleles fetched