Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.133461905C>A | CA463035369 | ST3GAL1 | c.819G>T (p.Ser273=) | |
8 | g.133461905C= | CA1821262814 | ST3GAL1 | c.819G= (p.Ser273=) | |
8 | g.133461905C>G | CA463035370 | ST3GAL1 | c.819G>C (p.Ser273=) | |
8 | g.133461905C>T | CA4887070 | ST3GAL1 | c.819G>A (p.Ser273=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.133461905_133461910delinsCGAGAG | CA1821262815 | ST3GAL1 | c.814_819delinsCTCTCG (p.Leu272=) | |
8 | g.133461906G>A | CA4887071 | ST3GAL1 | c.818C>T (p.Ser273Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
8 | g.133461906G>C | CA372258010 | ST3GAL1 | c.818C>G (p.Ser273Trp) | |
8 | g.133461906G= | CA1821262817 | ST3GAL1 | c.818C= (p.Ser273=) | |
8 | g.133461906G>T | CA372258011 | ST3GAL1 | c.818C>A (p.Ser273Ter) | gnomAD v4 |
8 | g.133461908_133461912del | CA1821262816 | ST3GAL1 | c.814_818del (p.Leu272GlyfsTer10) | dbSNP gnomAD v4 |
8 | g.133461907A>C | CA372258012 | ST3GAL1 | c.817T>G (p.Ser273Ala) | |
8 | g.133461907A>G | CA372258013 | ST3GAL1 | c.817T>C (p.Ser273Pro) | |
8 | g.133461907A>T | CA372258014 | ST3GAL1 | c.817T>A (p.Ser273Thr) | |
8 | g.133461908G>A | CA4887072 | ST3GAL1 | c.816C>T (p.Leu272=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.133461908G>C | CA186411697 | ST3GAL1 | c.816C>G (p.Leu272=) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.133461908G= | CA1821262818 | ST3GAL1 | c.816C= (p.Leu272=) | |
8 | g.133461908G>T | CA463035371 | ST3GAL1 | c.816C>A (p.Leu272=) | |
8 | g.133461909A= | CA1821262819 | ST3GAL1 | c.815T= (p.Leu272=) | |
8 | g.133461909A>C | CA372258015 | ST3GAL1 | c.815T>G (p.Leu272Arg) | |
8 | g.133461909A>G | CA372258016 | ST3GAL1 | c.815T>C (p.Leu272Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.133461909A>T | CA372258017 | ST3GAL1 | c.815T>A (p.Leu272His) | |
8 | g.133461910G>A | CA372258018 | ST3GAL1 | c.814C>T (p.Leu272Phe) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.133461910G>C | CA372258019 | ST3GAL1 | c.814C>G (p.Leu272Val) | |
8 | g.133461910G= | CA1821262820 | ST3GAL1 | c.814C= (p.Leu272=) | |
8 | g.133461910G>T | CA372258020 | ST3GAL1 | c.814C>A (p.Leu272Ile) | |
8 | g.133461911G>A | CA463035373 | ST3GAL1 | c.813C>T (p.Ile271=) | COSMIC |
8 | g.133461911G>C | CA186411703 | ST3GAL1 | c.813C>G (p.Ile271Met) | dbSNP |
8 | g.133461911G= | CA1821262821 | ST3GAL1 | c.813C= (p.Ile271=) | |
8 | g.133461911G>T | CA463035372 | ST3GAL1 | c.813C>A (p.Ile271=) | |
8 | g.133461912A>C | CA372258021 | ST3GAL1 | c.812T>G (p.Ile271Ser) | |
8 | g.133461912A>G | CA372258022 | ST3GAL1 | c.812T>C (p.Ile271Thr) | |
8 | g.133461912A>T | CA372258023 | ST3GAL1 | c.812T>A (p.Ile271Asn) | |
8 | g.133461913T>A | CA372258024 | ST3GAL1 | c.811A>T (p.Ile271Phe) | |
8 | g.133461913T>C | CA372258025 | ST3GAL1 | c.811A>G (p.Ile271Val) | |
8 | g.133461913T>G | CA372258026 | ST3GAL1 | c.811A>C (p.Ile271Leu) | |
8 | g.133461914G>A | CA463035376 | ST3GAL1 | c.810C>T (p.Gly270=) | dbSNP |
8 | g.133461914G>C | CA463035375 | ST3GAL1 | c.810C>G (p.Gly270=) | gnomAD v4 |
8 | g.133461914G= | CA1821262822 | ST3GAL1 | c.810C= (p.Gly270=) | |
8 | g.133461914G>T | CA463035374 | ST3GAL1 | c.810C>A (p.Gly270=) | gnomAD v4 |
8 | g.133461915C>A | CA372258027 | ST3GAL1 | c.809G>T (p.Gly270Val) | |
8 | g.133461915C= | CA1821262823 | ST3GAL1 | c.809G= (p.Gly270=) | |
8 | g.133461915C>G | CA4887074 | ST3GAL1 | c.809G>C (p.Gly270Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.133461915C>T | CA4887073 | ST3GAL1 | c.809G>A (p.Gly270Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.133461916C>A | CA372258028 | ST3GAL1 | c.808G>T (p.Gly270Cys) | |
8 | g.133461916C= | CA1821262824 | ST3GAL1 | c.808G= (p.Gly270=) | |
8 | g.133461916C>G | CA372258029 | ST3GAL1 | c.808G>C (p.Gly270Arg) | |
8 | g.133461916C>T | CA4887075 | ST3GAL1 | c.808G>A (p.Gly270Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
8 | g.133461917G>A | CA463035377 | ST3GAL1 | c.807C>T (p.Thr269=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
8 | g.133461917G>C | CA463035379 | ST3GAL1 | c.807C>G (p.Thr269=) | |
8 | g.133461917G= | CA1821262825 | ST3GAL1 | c.807C= (p.Thr269=) |