Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.153705065T>A | CA358497795 | TLR2 | c.2158T>A (p.Ser720Thr) c.436T>A (p.Ser146Thr) | |
4 | g.153705065T>C | CA358497798 | TLR2 | c.2158T>C (p.Ser720Pro) c.436T>C (p.Ser146Pro) | |
4 | g.153705065T>G | CA358497801 | TLR2 | c.2158T>G (p.Ser720Ala) c.436T>G (p.Ser146Ala) | |
4 | g.153705066C>A | CA358497802 | TLR2 | c.2159C>A (p.Ser720Tyr) c.437C>A (p.Ser146Tyr) | |
4 | g.153705066C= | CA1504541739 | TLR2 | c.2159C= (p.Ser720=) c.437C= (p.Ser146=) | |
4 | g.153705066C>G | CA358497804 | TLR2 | c.2159C>G (p.Ser720Cys) c.437C>G (p.Ser146Cys) | dbSNP |
4 | g.153705066C>T | CA358497806 | TLR2 | c.2159C>T (p.Ser720Phe) c.437C>T (p.Ser146Phe) | dbSNP COSMIC |
4 | g.153705067C>A | CA442008568 | TLR2 | c.2160C>A (p.Ser720=) c.438C>A (p.Ser146=) | |
4 | g.153705067C>G | CA442008569 | TLR2 | c.2160C>G (p.Ser720=) c.438C>G (p.Ser146=) | |
4 | g.153705067C>T | CA442008567 | TLR2 | c.2160C>T (p.Ser720=) c.438C>T (p.Ser146=) | gnomAD v4 |
4 | g.153705068C>A | CA358497808 | TLR2 | c.2161C>A (p.His721Asn) c.439C>A (p.His147Asn) | gnomAD v4 |
4 | g.153705068C>G | CA358497813 | TLR2 | c.2161C>G (p.His721Asp) c.439C>G (p.His147Asp) | |
4 | g.153705068C>T | CA358497811 | TLR2 | c.2161C>T (p.His721Tyr) c.439C>T (p.His147Tyr) | |
4 | g.153705069A= | CA1504541741 | TLR2 | c.2162A= (p.His721=) c.440A= (p.His147=) | |
4 | g.153705069A>C | CA358497816 | TLR2 | c.2162A>C (p.His721Pro) c.440A>C (p.His147Pro) | gnomAD v4 |
4 | g.153705069A>G | CA108714259 | TLR2 | c.2162A>G (p.His721Arg) c.440A>G (p.His147Arg) | ClinVar dbSNP gnomAD v4 |
4 | g.153705069A>T | CA358497818 | TLR2 | c.2162A>T (p.His721Leu) c.440A>T (p.His147Leu) | |
4 | g.153705070T>A | CA358497821 | TLR2 | c.2163T>A (p.His721Gln) c.441T>A (p.His147Gln) | |
4 | g.153705070T>C | CA442008570 | TLR2 | c.2163T>C (p.His721=) c.441T>C (p.His147=) | |
4 | g.153705070T>G | CA358497822 | TLR2 | c.2163T>G (p.His721Gln) c.441T>G (p.His147Gln) | |
4 | g.153705071T>A | CA358497825 | TLR2 | c.2164T>A (p.Phe722Ile) c.442T>A (p.Phe148Ile) | |
4 | g.153705071T>C | CA358497826 | TLR2 | c.2164T>C (p.Phe722Leu) c.442T>C (p.Phe148Leu) | |
4 | g.153705071T>G | CA358497828 | TLR2 | c.2164T>G (p.Phe722Val) c.442T>G (p.Phe148Val) | |
4 | g.153705072T>A | CA358497832 | TLR2 | c.2165T>A (p.Phe722Tyr) c.443T>A (p.Phe148Tyr) | |
4 | g.153705072T>C | CA358497834 | TLR2 | c.2165T>C (p.Phe722Ser) c.443T>C (p.Phe148Ser) | |
4 | g.153705072T>G | CA358497835 | TLR2 | c.2165T>G (p.Phe722Cys) c.443T>G (p.Phe148Cys) | |
4 | g.153705073C>A | CA3111020 | TLR2 | c.2166C>A (p.Phe722Leu) c.444C>A (p.Phe148Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.153705073C= | CA1504541745 | TLR2 | c.2166C= (p.Phe722=) c.444C= (p.Phe148=) | |
4 | g.153705073C>G | CA358497839 | TLR2 | c.2166C>G (p.Phe722Leu) c.444C>G (p.Phe148Leu) | |
4 | g.153705073C>T | CA442008574 | TLR2 | c.2166C>T (p.Phe722=) c.444C>T (p.Phe148=) | COSMIC |
4 | g.153705074C>A | CA3111021 | TLR2 | c.2167C>A (p.Arg723Ser) c.445C>A (p.Arg149Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.153705074C= | CA1504541746 | TLR2 | c.2167C= (p.Arg723=) c.445C= (p.Arg149=) | |
4 | g.153705074C>G | CA358497844 | TLR2 | c.2167C>G (p.Arg723Gly) c.445C>G (p.Arg149Gly) | |
4 | g.153705074C>T | CA3111022 | TLR2 | c.2167C>T (p.Arg723Cys) c.445C>T (p.Arg149Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.153705075G>A | CA3111023 | TLR2 | c.2168G>A (p.Arg723His) c.446G>A (p.Arg149His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
4 | g.153705075G>C | CA358497849 | TLR2 | c.2168G>C (p.Arg723Pro) c.446G>C (p.Arg149Pro) | |
4 | g.153705075G= | CA1504541748 | TLR2 | c.2168G= (p.Arg723=) c.446G= (p.Arg149=) | |
4 | g.153705075G>T | CA358497851 | TLR2 | c.2168G>T (p.Arg723Leu) c.446G>T (p.Arg149Leu) | gnomAD v4 |
4 | g.153705076T>A | CA442008579 | TLR2 | c.2169T>A (p.Arg723=) c.447T>A (p.Arg149=) | |
4 | g.153705076T>C | CA3111024 | TLR2 | c.2169T>C (p.Arg723=) c.447T>C (p.Arg149=) | dbSNP ExAC |
4 | g.153705076T>G | CA442008581 | TLR2 | c.2169T>G (p.Arg723=) c.447T>G (p.Arg149=) | |
4 | g.153705076T= | CA1504541755 | TLR2 | c.2169T= (p.Arg723=) c.447T= (p.Arg149=) | |
4 | g.153705077C>A | CA358497854 | TLR2 | c.2170C>A (p.Leu724Ile) c.448C>A (p.Leu150Ile) | |
4 | g.153705077C>G | CA358497856 | TLR2 | c.2170C>G (p.Leu724Val) c.448C>G (p.Leu150Val) | |
4 | g.153705077C>T | CA358497859 | TLR2 | c.2170C>T (p.Leu724Phe) c.448C>T (p.Leu150Phe) | COSMIC |
4 | g.153705078T>A | CA358497861 | TLR2 | c.2171T>A (p.Leu724His) c.449T>A (p.Leu150His) | |
4 | g.153705078T>C | CA358497863 | TLR2 | c.2171T>C (p.Leu724Pro) c.449T>C (p.Leu150Pro) | |
4 | g.153705078T>G | CA358497864 | TLR2 | c.2171T>G (p.Leu724Arg) c.449T>G (p.Leu150Arg) | |
4 | g.153705079T>A | CA442008582 | TLR2 | c.2172T>A (p.Leu724=) c.450T>A (p.Leu150=) | |
4 | g.153705079T>C | CA3111025 | TLR2 | c.2172T>C (p.Leu724=) c.450T>C (p.Leu150=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |