Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.41972344T>ACA367321826GLI3c.2096A>T (p.Lys699Met)
c.1922A>T (p.Lys641Met)
n.2073A>T
c.1919A>T (p.Lys640Met)
c.2093A>T (p.Lys698Met)
7g.41972344T>CCA367321827GLI3c.2096A>G (p.Lys699Arg)
c.1922A>G (p.Lys641Arg)
n.2073A>G
c.1919A>G (p.Lys640Arg)
c.2093A>G (p.Lys698Arg)
7g.41972344T>GCA367321828GLI3c.2096A>C (p.Lys699Thr)
c.1922A>C (p.Lys641Thr)
n.2073A>C
c.1919A>C (p.Lys640Thr)
c.2093A>C (p.Lys698Thr)
7g.41972345T>ACA367321829GLI3c.2095A>T (p.Lys699Ter)
c.1921A>T (p.Lys641Ter)
n.2072A>T
c.1918A>T (p.Lys640Ter)
c.2092A>T (p.Lys698Ter)
7g.41972345T>CCA367321830GLI3c.2095A>G (p.Lys699Glu)
c.1921A>G (p.Lys641Glu)
n.2072A>G
c.1918A>G (p.Lys640Glu)
c.2092A>G (p.Lys698Glu)
7g.41972345T>GCA367321831GLI3c.2095A>C (p.Lys699Gln)
c.1921A>C (p.Lys641Gln)
n.2072A>C
c.1918A>C (p.Lys640Gln)
c.2092A>C (p.Lys698Gln)
7g.41972346C>ACA367321832GLI3c.2094G>T (p.Glu698Asp)
c.1920G>T (p.Glu640Asp)
n.2071G>T
c.1917G>T (p.Glu639Asp)
c.2091G>T (p.Glu697Asp)
7g.41972346C=CA1702647636GLI3c.2094G= (p.Glu698=)
c.1920G= (p.Glu640=)
n.2071G=
c.1917G= (p.Glu639=)
c.2091G= (p.Glu697=)
7g.41972346C>GCA367321833GLI3c.2094G>C (p.Glu698Asp)
c.1920G>C (p.Glu640Asp)
n.2071G>C
c.1917G>C (p.Glu639Asp)
c.2091G>C (p.Glu697Asp)
7g.41972346C>TCA4230692GLI3c.2094G>A (p.Glu698=)
c.1920G>A (p.Glu640=)
n.2071G>A
c.1917G>A (p.Glu639=)
c.2091G>A (p.Glu697=)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.41972347T>ACA367321834GLI3c.2093A>T (p.Glu698Val)
c.1919A>T (p.Glu640Val)
n.2070A>T
c.1916A>T (p.Glu639Val)
c.2090A>T (p.Glu697Val)
7g.41972347T>CCA367321835GLI3c.2093A>G (p.Glu698Gly)
c.1919A>G (p.Glu640Gly)
n.2070A>G
c.1916A>G (p.Glu639Gly)
c.2090A>G (p.Glu697Gly)
dbSNP gnomAD v2 gnomAD v4
7g.41972347T>GCA367321836GLI3c.2093A>C (p.Glu698Ala)
c.1919A>C (p.Glu640Ala)
n.2070A>C
c.1916A>C (p.Glu639Ala)
c.2090A>C (p.Glu697Ala)
7g.41972347T=CA1702647637GLI3c.2093A= (p.Glu698=)
c.1919A= (p.Glu640=)
n.2070A=
c.1916A= (p.Glu639=)
c.2090A= (p.Glu697=)
7g.41972348C>ACA367321839GLI3c.2092G>T (p.Glu698Ter)
c.1918G>T (p.Glu640Ter)
n.2069G>T
c.1915G>T (p.Glu639Ter)
c.2089G>T (p.Glu697Ter)
7g.41972348C>GCA367321837GLI3c.2092G>C (p.Glu698Gln)
c.1918G>C (p.Glu640Gln)
n.2069G>C
c.1915G>C (p.Glu639Gln)
c.2089G>C (p.Glu697Gln)
7g.41972348C>TCA367321838GLI3c.2092G>A (p.Glu698Lys)
c.1918G>A (p.Glu640Lys)
n.2069G>A
c.1915G>A (p.Glu639Lys)
c.2089G>A (p.Glu697Lys)
7g.41972349T>ACA454525400GLI3c.2091A>T (p.Ala697=)
c.1917A>T (p.Ala639=)
n.2068A>T
c.1914A>T (p.Ala638=)
c.2088A>T (p.Ala696=)
7g.41972349T>CCA454525401GLI3c.2091A>G (p.Ala697=)
c.1917A>G (p.Ala639=)
n.2068A>G
c.1914A>G (p.Ala638=)
c.2088A>G (p.Ala696=)
7g.41972349T>GCA454525402GLI3c.2091A>C (p.Ala697=)
c.1917A>C (p.Ala639=)
n.2068A>C
c.1914A>C (p.Ala638=)
c.2088A>C (p.Ala696=)
7g.41972350delCA2499218887GLI3c.2090del (p.Ala697GlufsTer5)
c.1916del (p.Ala639GlufsTer5)
n.2067del
c.1913del (p.Ala638GlufsTer5)
c.2087del (p.Ala696GlufsTer5)
ClinVar dbSNP
7g.41972350G>ACA367321840GLI3c.2090C>T (p.Ala697Val)
c.1916C>T (p.Ala639Val)
n.2067C>T
c.1913C>T (p.Ala638Val)
c.2087C>T (p.Ala696Val)
dbSNP gnomAD v4
7g.41972350G>CCA367321841GLI3c.2090C>G (p.Ala697Gly)
c.1916C>G (p.Ala639Gly)
n.2067C>G
c.1913C>G (p.Ala638Gly)
c.2087C>G (p.Ala696Gly)
7g.41972350G=CA1702647640GLI3c.2090C= (p.Ala697=)
c.1916C= (p.Ala639=)
n.2067C=
c.1913C= (p.Ala638=)
c.2087C= (p.Ala696=)
7g.41972350G>TCA367321842GLI3c.2090C>A (p.Ala697Glu)
c.1916C>A (p.Ala639Glu)
n.2067C>A
c.1913C>A (p.Ala638Glu)
c.2087C>A (p.Ala696Glu)
7g.41972351C>ACA367321843GLI3c.2089G>T (p.Ala697Ser)
c.1915G>T (p.Ala639Ser)
n.2066G>T
c.1912G>T (p.Ala638Ser)
c.2086G>T (p.Ala696Ser)
7g.41972351C>GCA367321844GLI3c.2089G>C (p.Ala697Pro)
c.1915G>C (p.Ala639Pro)
n.2066G>C
c.1912G>C (p.Ala638Pro)
c.2086G>C (p.Ala696Pro)
7g.41972351C>TCA367321845GLI3c.2089G>A (p.Ala697Thr)
c.1915G>A (p.Ala639Thr)
n.2066G>A
c.1912G>A (p.Ala638Thr)
c.2086G>A (p.Ala696Thr)
7g.41972352C>ACA367321846GLI3c.2088G>T (p.Lys696Asn)
c.1914G>T (p.Lys638Asn)
n.2065G>T
c.1911G>T (p.Lys637Asn)
c.2085G>T (p.Lys695Asn)
7g.41972352C>GCA367321847GLI3c.2088G>C (p.Lys696Asn)
c.1914G>C (p.Lys638Asn)
n.2065G>C
c.1911G>C (p.Lys637Asn)
c.2085G>C (p.Lys695Asn)
7g.41972352C>TCA454525407GLI3c.2088G>A (p.Lys696=)
c.1914G>A (p.Lys638=)
n.2065G>A
c.1911G>A (p.Lys637=)
c.2085G>A (p.Lys695=)
7g.41972353T>ACA367321848GLI3c.2087A>T (p.Lys696Met)
c.1913A>T (p.Lys638Met)
n.2064A>T
c.1910A>T (p.Lys637Met)
c.2084A>T (p.Lys695Met)
7g.41972353T>CCA367321849GLI3c.2087A>G (p.Lys696Arg)
c.1913A>G (p.Lys638Arg)
n.2064A>G
c.1910A>G (p.Lys637Arg)
c.2084A>G (p.Lys695Arg)
7g.41972353T>GCA367321850GLI3c.2087A>C (p.Lys696Thr)
c.1913A>C (p.Lys638Thr)
n.2064A>C
c.1910A>C (p.Lys637Thr)
c.2084A>C (p.Lys695Thr)
7g.41972354T>ACA367321852GLI3c.2086A>T (p.Lys696Ter)
c.1912A>T (p.Lys638Ter)
n.2063A>T
c.1909A>T (p.Lys637Ter)
c.2083A>T (p.Lys695Ter)
7g.41972354T>CCA367321851GLI3c.2086A>G (p.Lys696Glu)
c.1912A>G (p.Lys638Glu)
n.2063A>G
c.1909A>G (p.Lys637Glu)
c.2083A>G (p.Lys695Glu)
gnomAD v4
7g.41972354T>GCA4230693GLI3c.2086A>C (p.Lys696Gln)
c.1912A>C (p.Lys638Gln)
n.2063A>C
c.1909A>C (p.Lys637Gln)
c.2083A>C (p.Lys695Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.41972354T=CA1702647643GLI3c.2086A= (p.Lys696=)
c.1912A= (p.Lys638=)
n.2063A=
c.1909A= (p.Lys637=)
c.2083A= (p.Lys695=)
7g.41972355G>ACA454525413GLI3c.2085C>T (p.Val695=)
c.1911C>T (p.Val637=)
n.2062C>T
c.1908C>T (p.Val636=)
c.2082C>T (p.Val694=)
7g.41972355G>CCA454525415GLI3c.2085C>G (p.Val695=)
c.1911C>G (p.Val637=)
n.2062C>G
c.1908C>G (p.Val636=)
c.2082C>G (p.Val694=)
gnomAD v4
7g.41972355G=CA1702647646GLI3c.2085C= (p.Val695=)
c.1911C= (p.Val637=)
n.2062C=
c.1908C= (p.Val636=)
c.2082C= (p.Val694=)
7g.41972355G>TCA454525418GLI3c.2085C>A (p.Val695=)
c.1911C>A (p.Val637=)
n.2062C>A
c.1908C>A (p.Val636=)
c.2082C>A (p.Val694=)
dbSNP gnomAD v3 gnomAD v4
7g.41972356A>CCA367321853GLI3c.2084T>G (p.Val695Gly)
c.1910T>G (p.Val637Gly)
n.2061T>G
c.1907T>G (p.Val636Gly)
c.2081T>G (p.Val694Gly)
7g.41972356A>GCA367321854GLI3c.2084T>C (p.Val695Ala)
c.1910T>C (p.Val637Ala)
n.2061T>C
c.1907T>C (p.Val636Ala)
c.2081T>C (p.Val694Ala)
7g.41972356A>TCA367321855GLI3c.2084T>A (p.Val695Asp)
c.1910T>A (p.Val637Asp)
n.2061T>A
c.1907T>A (p.Val636Asp)
c.2081T>A (p.Val694Asp)
7g.41972357C>ACA156913583GLI3c.2083G>T (p.Val695Phe)
c.1909G>T (p.Val637Phe)
n.2060G>T
c.1906G>T (p.Val636Phe)
c.2080G>T (p.Val694Phe)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.41972357C=CA1702647650GLI3c.2083G= (p.Val695=)
c.1909G= (p.Val637=)
n.2060G=
c.1906G= (p.Val636=)
c.2080G= (p.Val694=)
7g.41972357C>GCA367321856GLI3c.2083G>C (p.Val695Leu)
c.1909G>C (p.Val637Leu)
n.2060G>C
c.1906G>C (p.Val636Leu)
c.2080G>C (p.Val694Leu)
dbSNP
7g.41972357C>TCA4230694GLI3c.2083G>A (p.Val695Ile)
c.1909G>A (p.Val637Ile)
n.2060G>A
c.1906G>A (p.Val636Ile)
c.2080G>A (p.Val694Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
7g.41972357_41972358delinsGGCTTCTCTCA2695207655GLI3c.2082_2083delinsAGAGAAGCC (p.Val695GlufsTer?)
c.1908_1909delinsAGAGAAGCC (p.Val637GlufsTer?)
n.2059_2060delinsAGAGAAGCC
c.1905_1906delinsAGAGAAGCC (p.Val636GlufsTer?)
c.2079_2080delinsAGAGAAGCC (p.Val694GlufsTer?)

Number of alleles fetched