| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.161673964C>A | CA421420323 | FCGR2B | c.651C>A (p.Pro217=) c.630C>A (p.Pro210=) n.701C>A n.2019C>A c.648C>A (p.Pro216=) c.627C>A (p.Pro209=) n.880C>A | |
| 1 | g.161673964C>G | CA421420325 | FCGR2B | c.651C>G (p.Pro217=) c.630C>G (p.Pro210=) n.701C>G n.2019C>G c.648C>G (p.Pro216=) c.627C>G (p.Pro209=) n.880C>G | |
| 1 | g.161673964C>T | CA421420327 | FCGR2B | c.651C>T (p.Pro217=) c.630C>T (p.Pro210=) n.701C>T n.2019C>T c.648C>T (p.Pro216=) c.627C>T (p.Pro209=) n.880C>T | |
| 1 | g.161673965A>C | CA343367451 | FCGR2B | c.652A>C (p.Ser218Arg) c.631A>C (p.Ser211Arg) n.702A>C n.2020A>C c.649A>C (p.Ser217Arg) c.628A>C (p.Ser210Arg) n.881A>C | |
| 1 | g.161673965A>G | CA343367454 | FCGR2B | c.652A>G (p.Ser218Gly) c.631A>G (p.Ser211Gly) n.702A>G n.2020A>G c.649A>G (p.Ser217Gly) c.628A>G (p.Ser210Gly) n.881A>G | |
| 1 | g.161673965A>T | CA343367457 | FCGR2B | c.652A>T (p.Ser218Cys) c.631A>T (p.Ser211Cys) n.702A>T n.2020A>T c.649A>T (p.Ser217Cys) c.628A>T (p.Ser210Cys) n.881A>T | |
| 1 | g.161673966G>A | CA343367461 | FCGR2B | c.653G>A (p.Ser218Asn) c.632G>A (p.Ser211Asn) n.703G>A n.2021G>A c.650G>A (p.Ser217Asn) c.629G>A (p.Ser210Asn) n.882G>A | |
| 1 | g.161673966G>C | CA343367463 | FCGR2B | c.653G>C (p.Ser218Thr) c.632G>C (p.Ser211Thr) n.703G>C n.2021G>C c.650G>C (p.Ser217Thr) c.629G>C (p.Ser210Thr) n.882G>C | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.161673966G= | CA1202839737 | FCGR2B | c.653G= (p.Ser218=) c.632G= (p.Ser211=) n.703G= n.2021G= c.650G= (p.Ser217=) c.629G= (p.Ser210=) n.882G= | |
| 1 | g.161673966G>T | CA343367465 | FCGR2B | c.653G>T (p.Ser218Ile) c.632G>T (p.Ser211Ile) n.703G>T n.2021G>T c.650G>T (p.Ser217Ile) c.629G>T (p.Ser210Ile) n.882G>T | |
| 1 | g.161673967C>A | CA343367466 | FCGR2B | c.654C>A (p.Ser218Arg) c.633C>A (p.Ser211Arg) n.704C>A n.2022C>A c.651C>A (p.Ser217Arg) c.630C>A (p.Ser210Arg) n.883C>A | |
| 1 | g.161673967C>G | CA343367467 | FCGR2B | c.654C>G (p.Ser218Arg) c.633C>G (p.Ser211Arg) n.704C>G n.2022C>G c.651C>G (p.Ser217Arg) c.630C>G (p.Ser210Arg) n.883C>G | |
| 1 | g.161673967C>T | CA421420337 | FCGR2B | c.654C>T (p.Ser218=) c.633C>T (p.Ser211=) n.704C>T n.2022C>T c.651C>T (p.Ser217=) c.630C>T (p.Ser210=) n.883C>T | |
| 1 | g.161673968T>A | CA343367472 | FCGR2B | c.655T>A (p.Ser219Thr) c.634T>A (p.Ser212Thr) n.705T>A n.2023T>A c.652T>A (p.Ser218Thr) c.631T>A (p.Ser211Thr) n.884T>A | |
| 1 | g.161673968T>C | CA343367471 | FCGR2B | c.655T>C (p.Ser219Pro) c.634T>C (p.Ser212Pro) n.705T>C n.2023T>C c.652T>C (p.Ser218Pro) c.631T>C (p.Ser211Pro) n.884T>C | |
| 1 | g.161673968T>G | CA343367469 | FCGR2B | c.655T>G (p.Ser219Ala) c.634T>G (p.Ser212Ala) n.705T>G n.2023T>G c.652T>G (p.Ser218Ala) c.631T>G (p.Ser211Ala) n.884T>G | |
| 1 | g.161673969C>A | CA343367475 | FCGR2B | c.656C>A (p.Ser219Tyr) c.635C>A (p.Ser212Tyr) n.706C>A n.2024C>A c.653C>A (p.Ser218Tyr) c.632C>A (p.Ser211Tyr) n.885C>A | |
| 1 | g.161673969C= | CA1202839738 | FCGR2B | c.656C= (p.Ser219=) c.635C= (p.Ser212=) n.706C= n.2024C= c.653C= (p.Ser218=) c.632C= (p.Ser211=) n.885C= | |
| 1 | g.161673969C>G | CA343367476 | FCGR2B | c.656C>G (p.Ser219Cys) c.635C>G (p.Ser212Cys) n.706C>G n.2024C>G c.653C>G (p.Ser218Cys) c.632C>G (p.Ser211Cys) n.885C>G | |
| 1 | g.161673969C>T | CA1212861 | FCGR2B | c.656C>T (p.Ser219Phe) c.635C>T (p.Ser212Phe) n.706C>T n.2024C>T c.653C>T (p.Ser218Phe) c.632C>T (p.Ser211Phe) n.885C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.161673970T>A | CA421420347 | FCGR2B | c.657T>A (p.Ser219=) c.636T>A (p.Ser212=) n.707T>A n.2025T>A c.654T>A (p.Ser218=) c.633T>A (p.Ser211=) n.886T>A | |
| 1 | g.161673970T>C | CA421420348 | FCGR2B | c.657T>C (p.Ser219=) c.636T>C (p.Ser212=) n.707T>C n.2025T>C c.654T>C (p.Ser218=) c.633T>C (p.Ser211=) n.886T>C | |
| 1 | g.161673970T>G | CA421420351 | FCGR2B | c.657T>G (p.Ser219=) c.636T>G (p.Ser212=) n.707T>G n.2025T>G c.654T>G (p.Ser218=) c.633T>G (p.Ser211=) n.886T>G | dbSNP |
| 1 | g.161673970T= | CA1202839739 | FCGR2B | c.657T= (p.Ser219=) c.636T= (p.Ser212=) n.707T= n.2025T= c.654T= (p.Ser218=) c.633T= (p.Ser211=) n.886T= | |
| 1 | g.161673971T>A | CA343367482 | FCGR2B | c.658T>A (p.Ser220Thr) c.637T>A (p.Ser213Thr) n.708T>A n.2026T>A c.655T>A (p.Ser219Thr) c.634T>A (p.Ser212Thr) n.887T>A | |
| 1 | g.161673971T>C | CA343367484 | FCGR2B | c.658T>C (p.Ser220Pro) c.637T>C (p.Ser213Pro) n.708T>C n.2026T>C c.655T>C (p.Ser219Pro) c.634T>C (p.Ser212Pro) n.887T>C | |
| 1 | g.161673971T>G | CA343367487 | FCGR2B | c.658T>G (p.Ser220Ala) c.637T>G (p.Ser213Ala) n.708T>G n.2026T>G c.655T>G (p.Ser219Ala) c.634T>G (p.Ser212Ala) n.887T>G | |
| 1 | g.161673972C>A | CA343367490 | FCGR2B | c.659C>A (p.Ser220Ter) c.638C>A (p.Ser213Ter) n.709C>A n.2027C>A c.656C>A (p.Ser219Ter) c.635C>A (p.Ser212Ter) n.888C>A | |
| 1 | g.161673972C>G | CA343367492 | FCGR2B | c.659C>G (p.Ser220Ter) c.638C>G (p.Ser213Ter) n.709C>G n.2027C>G c.656C>G (p.Ser219Ter) c.635C>G (p.Ser212Ter) n.888C>G | |
| 1 | g.161673972C>T | CA343367495 | FCGR2B | c.659C>T (p.Ser220Leu) c.638C>T (p.Ser213Leu) n.709C>T n.2027C>T c.656C>T (p.Ser219Leu) c.635C>T (p.Ser212Leu) n.888C>T | gnomAD v4 |
| 1 | g.161673973A= | CA1202839740 | FCGR2B | c.660A= (p.Ser220=) c.639A= (p.Ser213=) n.710A= n.2028A= c.657A= (p.Ser219=) c.636A= (p.Ser212=) n.889A= | |
| 1 | g.161673973A>C | CA421420366 | FCGR2B | c.660A>C (p.Ser220=) c.639A>C (p.Ser213=) n.710A>C n.2028A>C c.657A>C (p.Ser219=) c.636A>C (p.Ser212=) n.889A>C | dbSNP |
| 1 | g.161673973A>G | CA421420364 | FCGR2B | c.660A>G (p.Ser220=) c.639A>G (p.Ser213=) n.710A>G n.2028A>G c.657A>G (p.Ser219=) c.636A>G (p.Ser212=) n.889A>G | |
| 1 | g.161673973A>T | CA421420362 | FCGR2B | c.660A>T (p.Ser220=) c.639A>T (p.Ser213=) n.710A>T n.2028A>T c.657A>T (p.Ser219=) c.636A>T (p.Ser212=) n.889A>T | |
| 1 | g.161673974C>A | CA343367497 | FCGR2B | c.661C>A (p.Pro221Thr) c.640C>A (p.Pro214Thr) n.711C>A n.2029C>A c.658C>A (p.Pro220Thr) c.637C>A (p.Pro213Thr) n.890C>A | gnomAD v4 |
| 1 | g.161673974C>G | CA343367499 | FCGR2B | c.661C>G (p.Pro221Ala) c.640C>G (p.Pro214Ala) n.711C>G n.2029C>G c.658C>G (p.Pro220Ala) c.637C>G (p.Pro213Ala) n.890C>G | |
| 1 | g.161673974C>T | CA343367501 | FCGR2B | c.661C>T (p.Pro221Ser) c.640C>T (p.Pro214Ser) n.711C>T n.2029C>T c.658C>T (p.Pro220Ser) c.637C>T (p.Pro213Ser) n.890C>T | |
| 1 | g.161673975C>A | CA343367516 | FCGR2B | c.662C>A (p.Pro221Gln) c.641C>A (p.Pro214Gln) n.712C>A n.2030C>A c.659C>A (p.Pro220Gln) c.638C>A (p.Pro213Gln) n.891C>A | |
| 1 | g.161673975C= | CA1202839741 | FCGR2B | c.662C= (p.Pro221=) c.641C= (p.Pro214=) n.712C= n.2030C= c.659C= (p.Pro220=) c.638C= (p.Pro213=) n.891C= | |
| 1 | g.161673975C>G | CA343367505 | FCGR2B | c.662C>G (p.Pro221Arg) c.641C>G (p.Pro214Arg) n.712C>G n.2030C>G c.659C>G (p.Pro220Arg) c.638C>G (p.Pro213Arg) n.891C>G | |
| 1 | g.161673975C>T | CA343367503 | FCGR2B | c.662C>T (p.Pro221Leu) c.641C>T (p.Pro214Leu) n.712C>T n.2030C>T c.659C>T (p.Pro220Leu) c.638C>T (p.Pro213Leu) n.891C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 1 | g.161673976G>A | CA421420376 | FCGR2B | c.663G>A (p.Pro221=) c.642G>A (p.Pro214=) n.713G>A n.2031G>A c.660G>A (p.Pro220=) c.639G>A (p.Pro213=) n.892G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161673976G>C | CA421420378 | FCGR2B | c.663G>C (p.Pro221=) c.642G>C (p.Pro214=) n.713G>C n.2031G>C c.660G>C (p.Pro220=) c.639G>C (p.Pro213=) n.892G>C | |
| 1 | g.161673976G= | CA1202839742 | FCGR2B | c.663G= (p.Pro221=) c.642G= (p.Pro214=) n.713G= n.2031G= c.660G= (p.Pro220=) c.639G= (p.Pro213=) n.892G= | |
| 1 | g.161673976G>T | CA421420381 | FCGR2B | c.663G>T (p.Pro221=) c.642G>T (p.Pro214=) n.713G>T n.2031G>T c.660G>T (p.Pro220=) c.639G>T (p.Pro213=) n.892G>T | dbSNP gnomAD v4 |
| 1 | g.161673977A= | CA1202839743 | FCGR2B | c.664A= (p.Met222=) c.643A= (p.Met215=) n.714A= n.2032A= c.661A= (p.Met221=) c.640A= (p.Met214=) n.893A= | |
| 1 | g.161673977A>C | CA343367521 | FCGR2B | c.664A>C (p.Met222Leu) c.643A>C (p.Met215Leu) n.714A>C n.2032A>C c.661A>C (p.Met221Leu) c.640A>C (p.Met214Leu) n.893A>C | |
| 1 | g.161673977A>G | CA343367518 | FCGR2B | c.664A>G (p.Met222Val) c.643A>G (p.Met215Val) n.714A>G n.2032A>G c.661A>G (p.Met221Val) c.640A>G (p.Met214Val) n.893A>G | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.161673977A>T | CA343367519 | FCGR2B | c.664A>T (p.Met222Leu) c.643A>T (p.Met215Leu) n.714A>T n.2032A>T c.661A>T (p.Met221Leu) c.640A>T (p.Met214Leu) n.893A>T | |
| 1 | g.161673978T>A | CA343367525 | FCGR2B | c.665T>A (p.Met222Lys) c.644T>A (p.Met215Lys) n.715T>A n.2033T>A c.662T>A (p.Met221Lys) c.641T>A (p.Met214Lys) n.894T>A |