| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.43162826C>A | CA514828347 | TSPO | c.345C>A (p.Val115=) c.33C>A (p.Val11=) n.254C>A n.209C>A | gnomAD v4 |
| 22 | g.43162826C= | CA2407104063 | TSPO | c.345C= (p.Val115=) c.33C= (p.Val11=) n.254C= n.209C= | |
| 22 | g.43162826C>G | CA514828348 | TSPO | c.345C>G (p.Val115=) c.33C>G (p.Val11=) n.254C>G n.209C>G | |
| 22 | g.43162826C>T | CA514828349 | TSPO | c.345C>T (p.Val115=) c.33C>T (p.Val11=) n.254C>T n.209C>T | dbSNP gnomAD v2 gnomAD v4 |
| 22 | g.43162827A>C | CA411816896 | TSPO | c.346A>C (p.Ser116Arg) c.34A>C (p.Ser12Arg) n.255A>C n.210A>C | |
| 22 | g.43162827A>G | CA411816897 | TSPO | c.346A>G (p.Ser116Gly) c.34A>G (p.Ser12Gly) n.255A>G n.210A>G | gnomAD v4 |
| 22 | g.43162827A>T | CA411816898 | TSPO | c.346A>T (p.Ser116Cys) c.34A>T (p.Ser12Cys) n.255A>T n.210A>T | |
| 22 | g.43162828G>A | CA411816899 | TSPO | c.347G>A (p.Ser116Asn) c.35G>A (p.Ser12Asn) n.256G>A n.211G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.43162828G>C | CA411816900 | TSPO | c.347G>C (p.Ser116Thr) c.35G>C (p.Ser12Thr) n.256G>C n.211G>C | |
| 22 | g.43162828G= | CA2407104064 | TSPO | c.347G= (p.Ser116=) c.35G= (p.Ser12=) n.256G= n.211G= | |
| 22 | g.43162828G>T | CA411816901 | TSPO | c.347G>T (p.Ser116Ile) c.35G>T (p.Ser12Ile) n.256G>T n.211G>T | gnomAD v4 |
| 22 | g.43162829T>A | CA411816902 | TSPO | c.348T>A (p.Ser116Arg) c.36T>A (p.Ser12Arg) n.257T>A n.212T>A | gnomAD v4 |
| 22 | g.43162829T>C | CA514828350 | TSPO | c.348T>C (p.Ser116=) c.36T>C (p.Ser12=) n.257T>C n.212T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.43162829T>G | CA411816903 | TSPO | c.348T>G (p.Ser116Arg) c.36T>G (p.Ser12Arg) n.257T>G n.212T>G | dbSNP |
| 22 | g.43162829T= | CA2407104066 | TSPO | c.348T= (p.Ser116=) c.36T= (p.Ser12=) n.257T= n.212T= | |
| 22 | g.43162829dup | CA2407104065 | TSPO | c.348dup (p.Gly117TrpfsTer?) c.36dup (p.Gly13TrpfsTer?) n.257dup n.212dup | dbSNP |
| 22 | g.43162830G>A | CA411816904 | TSPO | c.349G>A (p.Gly117Arg) c.37G>A (p.Gly13Arg) n.258G>A n.213G>A | gnomAD v4 |
| 22 | g.43162830G>C | CA411816905 | TSPO | c.349G>C (p.Gly117Arg) c.37G>C (p.Gly13Arg) n.258G>C n.213G>C | dbSNP gnomAD v3 gnomAD v4 |
| 22 | g.43162830G= | CA2407104067 | TSPO | c.349G= (p.Gly117=) c.37G= (p.Gly13=) n.258G= n.213G= | |
| 22 | g.43162830G>T | CA411816906 | TSPO | c.349G>T (p.Gly117Trp) c.37G>T (p.Gly13Trp) n.258G>T n.213G>T | |
| 22 | g.43162831G>A | CA411816909 | TSPO | c.350G>A (p.Gly117Glu) c.38G>A (p.Gly13Glu) n.259G>A n.214G>A | dbSNP gnomAD v2 gnomAD v4 |
| 22 | g.43162831G>C | CA411816908 | TSPO | c.350G>C (p.Gly117Ala) c.38G>C (p.Gly13Ala) n.259G>C n.214G>C | |
| 22 | g.43162831G= | CA2407104068 | TSPO | c.350G= (p.Gly117=) c.38G= (p.Gly13=) n.259G= n.214G= | |
| 22 | g.43162831G>T | CA411816907 | TSPO | c.350G>T (p.Gly117Val) c.38G>T (p.Gly13Val) n.259G>T n.214G>T | gnomAD v4 |
| 22 | g.43162832G>A | CA514828351 | TSPO | c.351G>A (p.Gly117=) c.39G>A (p.Gly13=) n.260G>A n.215G>A | gnomAD v4 |
| 22 | g.43162832G>C | CA514828352 | TSPO | c.351G>C (p.Gly117=) c.39G>C (p.Gly13=) n.260G>C n.215G>C | |
| 22 | g.43162832G>T | CA514828353 | TSPO | c.351G>T (p.Gly117=) c.39G>T (p.Gly13=) n.260G>T n.215G>T | gnomAD v4 |
| 22 | g.43162833G>A | CA411816910 | TSPO | c.352G>A (p.Ala118Thr) c.40G>A (p.Ala14Thr) n.261G>A n.216G>A | gnomAD v4 |
| 22 | g.43162833G>C | CA411816911 | TSPO | c.352G>C (p.Ala118Pro) c.40G>C (p.Ala14Pro) n.261G>C n.216G>C | gnomAD v4 |
| 22 | g.43162833G>T | CA411816912 | TSPO | c.352G>T (p.Ala118Ser) c.40G>T (p.Ala14Ser) n.261G>T n.216G>T | |
| 22 | g.43162834C>A | CA411816913 | TSPO | c.353C>A (p.Ala118Glu) c.41C>A (p.Ala14Glu) n.262C>A n.217C>A | gnomAD v4 |
| 22 | g.43162834C= | CA2407104069 | TSPO | c.353C= (p.Ala118=) c.41C= (p.Ala14=) n.262C= n.217C= | |
| 22 | g.43162834C>G | CA411816914 | TSPO | c.353C>G (p.Ala118Gly) c.41C>G (p.Ala14Gly) n.262C>G n.217C>G | |
| 22 | g.43162834C>T | CA411816915 | TSPO | c.353C>T (p.Ala118Val) c.41C>T (p.Ala14Val) n.262C>T n.217C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.43162835G>A | CA10272821 | TSPO | c.354G>A (p.Ala118=) c.42G>A (p.Ala14=) n.263G>A n.218G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 22 | g.43162835G>C | CA514828355 | TSPO | c.354G>C (p.Ala118=) c.42G>C (p.Ala14=) n.263G>C n.218G>C | |
| 22 | g.43162835G= | CA2407104070 | TSPO | c.354G= (p.Ala118=) c.42G= (p.Ala14=) n.263G= n.218G= | |
| 22 | g.43162835G>T | CA514828354 | TSPO | c.354G>T (p.Ala118=) c.42G>T (p.Ala14=) n.263G>T n.218G>T | dbSNP gnomAD v2 gnomAD v4 |
| 22 | g.43162836G>A | CA411816916 | TSPO | c.355G>A (p.Ala119Thr) c.43G>A (p.Ala15Thr) n.264G>A n.219G>A | |
| 22 | g.43162836G>C | CA411816917 | TSPO | c.355G>C (p.Ala119Pro) c.43G>C (p.Ala15Pro) n.264G>C n.219G>C | |
| 22 | g.43162836G>T | CA411816918 | TSPO | c.355G>T (p.Ala119Ser) c.43G>T (p.Ala15Ser) n.264G>T n.219G>T | |
| 22 | g.43162837C>A | CA411816919 | TSPO | c.356C>A (p.Ala119Glu) c.44C>A (p.Ala15Glu) n.265C>A n.220C>A | gnomAD v4 |
| 22 | g.43162837C= | CA2407104071 | TSPO | c.356C= (p.Ala119=) c.44C= (p.Ala15=) n.265C= n.220C= | |
| 22 | g.43162837C>G | CA411816920 | TSPO | c.356C>G (p.Ala119Gly) c.44C>G (p.Ala15Gly) n.265C>G n.220C>G | |
| 22 | g.43162837C>T | CA10272822 | TSPO | c.356C>T (p.Ala119Val) c.44C>T (p.Ala15Val) n.265C>T n.220C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.43162838G>A | CA10272823 | TSPO | c.357G>A (p.Ala119=) c.45G>A (p.Ala15=) n.266G>A n.221G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 22 | g.43162838G>C | CA514828356 | TSPO | c.357G>C (p.Ala119=) c.45G>C (p.Ala15=) n.266G>C n.221G>C | gnomAD v4 |
| 22 | g.43162838G= | CA2407104072 | TSPO | c.357G= (p.Ala119=) c.45G= (p.Ala15=) n.266G= n.221G= | |
| 22 | g.43162838G>T | CA514828357 | TSPO | c.357G>T (p.Ala119=) c.45G>T (p.Ala15=) n.266G>T n.221G>T | |
| 22 | g.43162839G>A | CA411816922 | TSPO | c.358G>A (p.Ala120Thr) c.46G>A (p.Ala16Thr) n.267G>A n.222G>A | gnomAD v4 |