Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.49621879C>ACA389619543MGAT2c.611C>A (p.Ala204Asp)
14g.49621879C=CA2135804724MGAT2c.611C= (p.Ala204=)
14g.49621879C>GCA389619545MGAT2c.611C>G (p.Ala204Gly)
gnomAD v4
14g.49621879C>TCA389619547MGAT2c.611C>T (p.Ala204Val)
dbSNP gnomAD v2 gnomAD v4
14g.49621880C>ACA486350331MGAT2c.612C>A (p.Ala204=)
COSMIC
14g.49621880C=CA2135804725MGAT2c.612C= (p.Ala204=)
14g.49621880C>GCA486350332MGAT2c.612C>G (p.Ala204=)
14g.49621880C>TCA260660733MGAT2c.612C>T (p.Ala204=)
dbSNP gnomAD v4
14g.49621881G>ACA389619552MGAT2c.613G>A (p.Ala205Thr)
gnomAD v4
14g.49621881G>CCA389619550MGAT2c.613G>C (p.Ala205Pro)
gnomAD v4
14g.49621881G>TCA389619548MGAT2c.613G>T (p.Ala205Ser)
14g.49621882C>ACA389619554MGAT2c.614C>A (p.Ala205Asp)
14g.49621882C>GCA389619556MGAT2c.614C>G (p.Ala205Gly)
14g.49621882C>TCA389619557MGAT2c.614C>T (p.Ala205Val)
14g.49621883T>ACA486350336MGAT2c.615T>A (p.Ala205=)
14g.49621883T>CCA486350338MGAT2c.615T>C (p.Ala205=)
gnomAD v4
14g.49621883T>GCA486350339MGAT2c.615T>G (p.Ala205=)
14g.49621884T>ACA389619559MGAT2c.616T>A (p.Leu206Met)
14g.49621884T>CCA486350340MGAT2c.616T>C (p.Leu206=)
dbSNP
14g.49621884T>GCA260660736MGAT2c.616T>G (p.Leu206Val)
dbSNP gnomAD v4
14g.49621884T=CA2135804726MGAT2c.616T= (p.Leu206=)
14g.49621885T>ACA389619561MGAT2c.617T>A (p.Leu206Ter)
14g.49621885T>CCA389619562MGAT2c.617T>C (p.Leu206Ser)
14g.49621885T>GCA389619564MGAT2c.617T>G (p.Leu206Trp)
14g.49621886G>ACA486350344MGAT2c.618G>A (p.Leu206=)
COSMIC
14g.49621886G>CCA389619565MGAT2c.618G>C (p.Leu206Phe)
14g.49621886G>TCA389619567MGAT2c.618G>T (p.Leu206Phe)
14g.49621887A>CCA389619568MGAT2c.619A>C (p.Lys207Gln)
14g.49621887A>GCA389619569MGAT2c.619A>G (p.Lys207Glu)
14g.49621887A>TCA389619570MGAT2c.619A>T (p.Lys207Ter)
14g.49621888A>CCA389619574MGAT2c.620A>C (p.Lys207Thr)
14g.49621888A>GCA389619571MGAT2c.620A>G (p.Lys207Arg)
14g.49621888A>TCA389619572MGAT2c.620A>T (p.Lys207Ile)
14g.49621889A=CA2135804727MGAT2c.621A= (p.Lys207=)
14g.49621889A>CCA389619575MGAT2c.621A>C (p.Lys207Asn)
14g.49621889A>GCA486350345MGAT2c.621A>G (p.Lys207=)
dbSNP
14g.49621889A>TCA389619577MGAT2c.621A>T (p.Lys207Asn)
14g.49621890T>ACA389619578MGAT2c.622T>A (p.Leu208Met)
14g.49621890T>CCA7172583MGAT2c.622T>C (p.Leu208=)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.49621890T>GCA389619581MGAT2c.622T>G (p.Leu208Val)
14g.49621890T=CA2135804728MGAT2c.622T= (p.Leu208=)
14g.49621891T>ACA389619582MGAT2c.623T>A (p.Leu208Ter)
14g.49621891T>CCA389619584MGAT2c.623T>C (p.Leu208Ser)
14g.49621891T>GCA389619585MGAT2c.623T>G (p.Leu208Trp)
14g.49621891_49621893delinsTGGCA2135804729MGAT2c.623_625delinsTGG (p.Leu208=)
14g.49621892G>ACA486350348MGAT2c.624G>A (p.Leu208=)
14g.49621892G>CCA389619586MGAT2c.624G>C (p.Leu208Phe)
14g.49621892G>TCA389619588MGAT2c.624G>T (p.Leu208Phe)
14g.49621894_49621895delCA706480752MGAT2c.626_627del (p.Gly209ValfsTer5)
dbSNP gnomAD v3 gnomAD v4
14g.49621893G>ACA389619589MGAT2c.625G>A (p.Gly209Arg)
gnomAD v4

Number of alleles fetched