Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.112446293T>A | CA386776155 | PTPN11 | c.32T>A (p.Ile11Asn) | |
12 | g.112446293T>C | CA386776154 | PTPN11 | c.32T>C (p.Ile11Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
12 | g.112446293T>G | CA386776153 | PTPN11 | c.32T>G (p.Ile11Ser) | |
12 | g.112446293T= | CA2063771364 | PTPN11 | c.32T= (p.Ile11=) | |
12 | g.112446294C>A | CA481880905 | PTPN11 | c.33C>A (p.Ile11=) | dbSNP |
12 | g.112446294C>G | CA386776156 | PTPN11 | c.33C>G (p.Ile11Met) | |
12 | g.112446294C>T | CA481880907 | PTPN11 | c.33C>T (p.Ile11=) | |
12 | g.112446295A= | CA2063771367 | PTPN11 | c.34A= (p.Thr12=) | |
12 | g.112446295A>C | CA386776157 | PTPN11 | c.34A>C (p.Thr12Pro) | |
12 | g.112446295A>G | CA386776158 | PTPN11 | c.34A>G (p.Thr12Ala) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
12 | g.112446295A>T | CA386776159 | PTPN11 | c.34A>T (p.Thr12Ser) | gnomAD v4 |
12 | g.112446296C>A | CA386776160 | PTPN11 | c.35C>A (p.Thr12Asn) | |
12 | g.112446296C>G | CA386776161 | PTPN11 | c.35C>G (p.Thr12Ser) | |
12 | g.112446296C>T | CA386776162 | PTPN11 | c.35C>T (p.Thr12Ile) | |
12 | g.112446297T>A | CA481880909 | PTPN11 | c.36T>A (p.Thr12=) | |
12 | g.112446297T>C | CA6798507 | PTPN11 | c.36T>C (p.Thr12=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.112446297T>G | CA481880911 | PTPN11 | c.36T>G (p.Thr12=) | |
12 | g.112446297T= | CA2063771374 | PTPN11 | c.36T= (p.Thr12=) | |
12 | g.112446298G>A | CA386776163 | PTPN11 | c.37G>A (p.Gly13Ser) | dbSNP |
12 | g.112446298G>C | CA386776164 | PTPN11 | c.37G>C (p.Gly13Arg) | |
12 | g.112446298G>T | CA386776165 | PTPN11 | c.37G>T (p.Gly13Cys) | |
12 | g.112446299G>A | CA386776168 | PTPN11 | c.38G>A (p.Gly13Asp) | COSMIC |
12 | g.112446299G>C | CA386776167 | PTPN11 | c.38G>C (p.Gly13Ala) | |
12 | g.112446299G>T | CA386776166 | PTPN11 | c.38G>T (p.Gly13Val) | |
12 | g.112446300T>A | CA481880914 | PTPN11 | c.39T>A (p.Gly13=) | |
12 | g.112446300T>C | CA481880916 | PTPN11 | c.39T>C (p.Gly13=) | gnomAD v4 |
12 | g.112446300T>G | CA481880917 | PTPN11 | c.39T>G (p.Gly13=) | |
12 | g.112446301G>A | CA386776169 | PTPN11 | c.40G>A (p.Val14Met) | dbSNP |
12 | g.112446301G>C | CA386776170 | PTPN11 | c.40G>C (p.Val14Leu) | |
12 | g.112446301G>T | CA386776171 | PTPN11 | c.40G>T (p.Val14Leu) | |
12 | g.112446302T>A | CA386776172 | PTPN11 | c.41T>A (p.Val14Glu) | |
12 | g.112446302T>C | CA386776173 | PTPN11 | c.41T>C (p.Val14Ala) | |
12 | g.112446302T>G | CA386776174 | PTPN11 | c.41T>G (p.Val14Gly) | |
12 | g.112446303G>A | CA481880918 | PTPN11 | c.42G>A (p.Val14=) | ClinVar |
12 | g.112446303G>C | CA481880919 | PTPN11 | c.42G>C (p.Val14=) | |
12 | g.112446303G>T | CA481880920 | PTPN11 | c.42G>T (p.Val14=) | |
12 | g.112446304G>A | CA386776175 | PTPN11 | c.43G>A (p.Glu15Lys) | gnomAD v4 |
12 | g.112446304G>C | CA386776176 | PTPN11 | c.43G>C (p.Glu15Gln) | |
12 | g.112446304G>T | CA386776177 | PTPN11 | c.43G>T (p.Glu15Ter) | |
12 | g.112446305A>C | CA386776178 | PTPN11 | c.44A>C (p.Glu15Ala) | |
12 | g.112446305A>G | CA386776179 | PTPN11 | c.44A>G (p.Glu15Gly) | |
12 | g.112446305A>T | CA386776180 | PTPN11 | c.44A>T (p.Glu15Val) | |
12 | g.112446306G>A | CA481880922 | PTPN11 | c.45G>A (p.Glu15=) | gnomAD v4 |
12 | g.112446306G>C | CA386776182 | PTPN11 | c.45G>C (p.Glu15Asp) | |
12 | g.112446306G>T | CA386776181 | PTPN11 | c.45G>T (p.Glu15Asp) | |
12 | g.112446307G>A | CA386776183 | PTPN11 | c.46G>A (p.Ala16Thr) | dbSNP |
12 | g.112446307G>C | CA386776184 | PTPN11 | c.46G>C (p.Ala16Pro) | |
12 | g.112446307G>T | CA386776185 | PTPN11 | c.46G>T (p.Ala16Ser) | |
12 | g.112446308C>A | CA386776186 | PTPN11 | c.47C>A (p.Ala16Glu) | |
12 | g.112446308C>G | CA386776187 | PTPN11 | c.47C>G (p.Ala16Gly) | dbSNP |