Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.71994516G>ACA385782068TPH2c.1019G>A (p.Gly340Asp)
c.425G>A (p.Gly142Asp)
12g.71994516G>CCA385782069TPH2c.1019G>C (p.Gly340Ala)
c.425G>C (p.Gly142Ala)
12g.71994516G>TCA385782071TPH2c.1019G>T (p.Gly340Val)
c.425G>T (p.Gly142Val)
12g.71994517T>ACA480765010TPH2c.1020T>A (p.Gly340=)
c.426T>A (p.Gly142=)
12g.71994517T>CCA480765011TPH2c.1020T>C (p.Gly340=)
c.426T>C (p.Gly142=)
12g.71994517T>GCA480765012TPH2c.1020T>G (p.Gly340=)
c.426T>G (p.Gly142=)
12g.71994518C>ACA385782075TPH2c.1021C>A (p.Leu341Met)
c.427C>A (p.Leu143Met)
12g.71994518C=CA2045533090TPH2c.1021C= (p.Leu341=)
c.427C= (p.Leu143=)
12g.71994518C>GCA385782077TPH2c.1021C>G (p.Leu341Val)
c.427C>G (p.Leu143Val)
12g.71994518C>TCA480765013TPH2c.1021C>T (p.Leu341=)
c.427C>T (p.Leu143=)
dbSNP gnomAD v3 gnomAD v4
12g.71994518_71994519delinsCTCA2045533089TPH2c.1021_1022delinsCT (p.Leu341=)
c.427_428delinsCT (p.Leu143=)
12g.71994519delCA691590803TPH2c.1022del (p.Leu341ArgfsTer14)
c.428del (p.Leu143ArgfsTer14)
dbSNP gnomAD v4
12g.71994519T>ACA385782079TPH2c.1022T>A (p.Leu341Gln)
c.428T>A (p.Leu143Gln)
12g.71994519T>CCA385782082TPH2c.1022T>C (p.Leu341Pro)
c.428T>C (p.Leu143Pro)
12g.71994519T>GCA385782083TPH2c.1022T>G (p.Leu341Arg)
c.428T>G (p.Leu143Arg)
12g.71994520G>ACA480765014TPH2c.1023G>A (p.Leu341=)
c.429G>A (p.Leu143=)
12g.71994520G>CCA480765015TPH2c.1023G>C (p.Leu341=)
c.429G>C (p.Leu143=)
12g.71994520G>TCA480765016TPH2c.1023G>T (p.Leu341=)
c.429G>T (p.Leu143=)
COSMIC
12g.71994521G>ACA385782085TPH2c.1024G>A (p.Ala342Thr)
c.430G>A (p.Ala144Thr)
gnomAD v4
12g.71994521G>CCA385782087TPH2c.1024G>C (p.Ala342Pro)
c.430G>C (p.Ala144Pro)
12g.71994521G>TCA385782089TPH2c.1024G>T (p.Ala342Ser)
c.430G>T (p.Ala144Ser)
12g.71994522C>ACA6689955TPH2c.1025C>A (p.Ala342Glu)
c.431C>A (p.Ala144Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.71994522C=CA2045533091TPH2c.1025C= (p.Ala342=)
c.431C= (p.Ala144=)
12g.71994522C>GCA385782094TPH2c.1025C>G (p.Ala342Gly)
c.431C>G (p.Ala144Gly)
12g.71994522C>TCA6689954TPH2c.1025C>T (p.Ala342Val)
c.431C>T (p.Ala144Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.71994523G>ACA6689956TPH2c.1026G>A (p.Ala342=)
c.432G>A (p.Ala144=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.71994523G>CCA480765017TPH2c.1026G>C (p.Ala342=)
c.432G>C (p.Ala144=)
12g.71994523G=CA2045533092TPH2c.1026G= (p.Ala342=)
c.432G= (p.Ala144=)
12g.71994523G>TCA480765018TPH2c.1026G>T (p.Ala342=)
c.432G>T (p.Ala144=)
12g.71994524T>ACA385782101TPH2c.1027T>A (p.Ser343Thr)
c.433T>A (p.Ser145Thr)
12g.71994524T>CCA385782104TPH2c.1027T>C (p.Ser343Pro)
c.433T>C (p.Ser145Pro)
12g.71994524T>GCA385782106TPH2c.1027T>G (p.Ser343Ala)
c.433T>G (p.Ser145Ala)
12g.71994525C>ACA385782108TPH2c.1028C>A (p.Ser343Tyr)
c.434C>A (p.Ser145Tyr)
12g.71994525C>GCA385782111TPH2c.1028C>G (p.Ser343Cys)
c.434C>G (p.Ser145Cys)
12g.71994525C>TCA385782113TPH2c.1028C>T (p.Ser343Phe)
c.434C>T (p.Ser145Phe)
12g.71994526T>ACA480765019TPH2c.1029T>A (p.Ser343=)
c.435T>A (p.Ser145=)
12g.71994526T>CCA480765020TPH2c.1029T>C (p.Ser343=)
c.435T>C (p.Ser145=)
12g.71994526T>GCA480765021TPH2c.1029T>G (p.Ser343=)
c.435T>G (p.Ser145=)
12g.71994527C>ACA385782116TPH2c.1030C>A (p.Leu344Met)
c.436C>A (p.Leu146Met)
12g.71994527C>GCA385782117TPH2c.1030C>G (p.Leu344Val)
c.436C>G (p.Leu146Val)
12g.71994527C>TCA480765022TPH2c.1030C>T (p.Leu344=)
c.436C>T (p.Leu146=)
12g.71994528T>ACA385782120TPH2c.1031T>A (p.Leu344Gln)
c.437T>A (p.Leu146Gln)
12g.71994528T>CCA385782123TPH2c.1031T>C (p.Leu344Pro)
c.437T>C (p.Leu146Pro)
12g.71994528T>GCA385782126TPH2c.1031T>G (p.Leu344Arg)
c.437T>G (p.Leu146Arg)
COSMIC
12g.71994529G>ACA480765023TPH2c.1032G>A (p.Leu344=)
c.438G>A (p.Leu146=)
dbSNP gnomAD v4
12g.71994529G>CCA480765024TPH2c.1032G>C (p.Leu344=)
c.438G>C (p.Leu146=)
12g.71994529G=CA2045533093TPH2c.1032G= (p.Leu344=)
c.438G= (p.Leu146=)
12g.71994529G>TCA480765025TPH2c.1032G>T (p.Leu344=)
c.438G>T (p.Leu146=)
COSMIC
12g.71994530G>ACA385782136TPH2c.1033G>A (p.Gly345Arg)
c.439G>A (p.Gly147Arg)
gnomAD v4
12g.71994530G>CCA385782131TPH2c.1033G>C (p.Gly345Arg)
c.439G>C (p.Gly147Arg)

Number of alleles fetched