Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.91234711_91234758dupCA7308381GPR68c.298_345dup (p.Ile115_Ser116insLeuLeuTyrGluAsnIleTyrIleSerValGlyPheLeuCysCysIle)
c.328_375dup (p.Ile125_Ser126insLeuLeuTyrGluAsnIleTyrIleSerValGlyPheLeuCysCysIle)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.91234743T>ACA390606976GPR68c.308A>T (p.Glu103Val)
c.338A>T (p.Glu113Val)
14g.91234743T>CCA390606977GPR68c.308A>G (p.Glu103Gly)
c.338A>G (p.Glu113Gly)
14g.91234743T>GCA390606978GPR68c.308A>C (p.Glu103Ala)
c.338A>C (p.Glu113Ala)
14g.91234744C>ACA390606981GPR68c.307G>T (p.Glu103Ter)
c.337G>T (p.Glu113Ter)
gnomAD v4
14g.91234744C=CA2154863287GPR68c.307G= (p.Glu103=)
c.337G= (p.Glu113=)
14g.91234744C>GCA390606980GPR68c.307G>C (p.Glu103Gln)
c.337G>C (p.Glu113Gln)
14g.91234744C>TCA390606979GPR68c.307G>A (p.Glu103Lys)
c.337G>A (p.Glu113Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.91234745G>ACA265534252GPR68c.306C>T (p.Tyr102=)
c.336C>T (p.Tyr112=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.91234745G>CCA390606982GPR68c.306C>G (p.Tyr102Ter)
c.336C>G (p.Tyr112Ter)
dbSNP gnomAD v4
14g.91234745G=CA2154863288GPR68c.306C= (p.Tyr102=)
c.336C= (p.Tyr112=)
14g.91234745G>TCA390606983GPR68c.306C>A (p.Tyr102Ter)
c.336C>A (p.Tyr112Ter)
gnomAD v4
14g.91234745_91234746delCA913960379GPR68c.305_306del (p.Tyr102Ter)
c.335_336del (p.Tyr112Ter)
gnomAD v2 gnomAD v3 gnomAD v4
14g.91234746T>ACA390606984GPR68c.305A>T (p.Tyr102Phe)
c.335A>T (p.Tyr112Phe)
gnomAD v4
14g.91234746T>CCA390606985GPR68c.305A>G (p.Tyr102Cys)
c.335A>G (p.Tyr112Cys)
14g.91234746T>GCA390606986GPR68c.305A>C (p.Tyr102Ser)
c.335A>C (p.Tyr112Ser)
14g.91234747A=CA2154863289GPR68c.304T= (p.Tyr102=)
c.334T= (p.Tyr112=)
14g.91234747A>CCA390606987GPR68c.304T>G (p.Tyr102Asp)
c.334T>G (p.Tyr112Asp)
14g.91234747A>GCA390606988GPR68c.304T>C (p.Tyr102His)
c.334T>C (p.Tyr112His)
dbSNP gnomAD v4
14g.91234747A>TCA390606989GPR68c.304T>A (p.Tyr102Asn)
c.334T>A (p.Tyr112Asn)
14g.91234748C>ACA487828409GPR68c.303G>T (p.Leu101=)
c.333G>T (p.Leu111=)
gnomAD v4
14g.91234748C>GCA487828410GPR68c.303G>C (p.Leu101=)
c.333G>C (p.Leu111=)
14g.91234748C>TCA487828411GPR68c.303G>A (p.Leu101=)
c.333G>A (p.Leu111=)
14g.91234749A=CA2154863290GPR68c.302T= (p.Leu101=)
c.332T= (p.Leu111=)
14g.91234749A>CCA390606990GPR68c.302T>G (p.Leu101Arg)
c.332T>G (p.Leu111Arg)
14g.91234749A>GCA7308387GPR68c.302T>C (p.Leu101Pro)
c.332T>C (p.Leu111Pro)
dbSNP ExAC gnomAD v2
14g.91234749A>TCA390606991GPR68c.302T>A (p.Leu101Gln)
c.332T>A (p.Leu111Gln)
14g.91234749_91234752dupCA2626123452GPR68c.299_302dup (p.Tyr102ProfsTer?)
c.329_332dup (p.Tyr112ProfsTer?)
gnomAD v4
14g.91234753_91234755delCA645581836GPR68c.300_302del (p.Leu101del)
c.330_332del (p.Leu111del)
COSMIC
14g.91234750G>ACA487828415GPR68c.301C>T (p.Leu101=)
c.331C>T (p.Leu111=)
14g.91234750G>CCA390606992GPR68c.301C>G (p.Leu101Val)
c.331C>G (p.Leu111Val)
14g.91234750G>TCA390606993GPR68c.301C>A (p.Leu101Met)
c.331C>A (p.Leu111Met)
14g.91234751G>ACA7308388GPR68c.300C>T (p.Leu100=)
c.330C>T (p.Leu110=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.91234751G>CCA487828418GPR68c.300C>G (p.Leu100=)
c.330C>G (p.Leu110=)
14g.91234751G=CA2154863291GPR68c.300C= (p.Leu100=)
c.330C= (p.Leu110=)
14g.91234751G>TCA487828419GPR68c.300C>A (p.Leu100=)
c.330C>A (p.Leu110=)
14g.91234752A>CCA390606996GPR68c.299T>G (p.Leu100Arg)
c.329T>G (p.Leu110Arg)
14g.91234752A>GCA390606994GPR68c.299T>C (p.Leu100Pro)
c.329T>C (p.Leu110Pro)
14g.91234752A>TCA390606995GPR68c.299T>A (p.Leu100His)
c.329T>A (p.Leu110His)
14g.91234753G>ACA390606997GPR68c.298C>T (p.Leu100Phe)
c.328C>T (p.Leu110Phe)
dbSNP
14g.91234753G>CCA390606998GPR68c.298C>G (p.Leu100Val)
c.328C>G (p.Leu110Val)
14g.91234753G=CA2154863292GPR68c.298C= (p.Leu100=)
c.328C= (p.Leu110=)
14g.91234753G>TCA390606999GPR68c.298C>A (p.Leu100Ile)
c.328C>A (p.Leu110Ile)
14g.91234754G>ACA487828425GPR68c.297C>T (p.Ile99=)
c.327C>T (p.Ile109=)
dbSNP
14g.91234754G>CCA390607000GPR68c.297C>G (p.Ile99Met)
c.327C>G (p.Ile109Met)
14g.91234754G=CA2154863293GPR68c.297C= (p.Ile99=)
c.327C= (p.Ile109=)
14g.91234754G>TCA487828427GPR68c.297C>A (p.Ile99=)
c.327C>A (p.Ile109=)
14g.91234755A>CCA390607001GPR68c.296T>G (p.Ile99Ser)
c.326T>G (p.Ile109Ser)
14g.91234755A>GCA390607002GPR68c.296T>C (p.Ile99Thr)
c.326T>C (p.Ile109Thr)
14g.91234755A>TCA390607003GPR68c.296T>A (p.Ile99Asn)
c.326T>A (p.Ile109Asn)
gnomAD v4

Number of alleles fetched