Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.159320357G>A | CA362032481 | IL12B | c.16C>T (p.His6Tyr) c.*141C>T (n.*141C>T) c.646C>T (p.His216Tyr) | |
5 | g.159320357G>C | CA362032482 | IL12B | c.16C>G (p.His6Asp) c.*141C>G (n.*141C>G) c.646C>G (p.His216Asp) | |
5 | g.159320357G>T | CA362032484 | IL12B | c.16C>A (p.His6Asn) c.*141C>A (n.*141C>A) c.646C>A (p.His216Asn) | |
5 | g.159320358A>C | CA447510871 | IL12B | c.15T>G (p.Val5=) c.*140T>G (n.*140T>G) c.645T>G (p.Val215=) | |
5 | g.159320358A>G | CA447510869 | IL12B | c.15T>C (p.Val5=) c.*140T>C (n.*140T>C) c.645T>C (p.Val215=) | |
5 | g.159320358A>T | CA447510867 | IL12B | c.15T>A (p.Val5=) c.*140T>A (n.*140T>A) c.645T>A (p.Val215=) | |
5 | g.159320359A>C | CA362032486 | IL12B | c.14T>G (p.Val5Gly) c.*139T>G (n.*139T>G) c.644T>G (p.Val215Gly) | |
5 | g.159320359A>G | CA362032488 | IL12B | c.14T>C (p.Val5Ala) c.*139T>C (n.*139T>C) c.644T>C (p.Val215Ala) | gnomAD v4 |
5 | g.159320359A>T | CA362032489 | IL12B | c.14T>A (p.Val5Asp) c.*139T>A (n.*139T>A) c.644T>A (p.Val215Asp) | |
5 | g.159320360C>A | CA362032492 | IL12B | c.13G>T (p.Val5Phe) c.*138G>T (n.*138G>T) c.643G>T (p.Val215Phe) | COSMIC COSMIC |
5 | g.159320360C= | CA1595017267 | IL12B | c.13G= (p.Val5=) c.*138G= (n.*138G=) c.643G= (p.Val215=) | |
5 | g.159320360C>G | CA362032494 | IL12B | c.13G>C (p.Val5Leu) c.*138G>C (n.*138G>C) c.643G>C (p.Val215Leu) | |
5 | g.159320360C>T | CA3538752 | IL12B | c.13G>A (p.Val5Ile) c.*138G>A (n.*138G>A) c.643G>A (p.Val215Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.159320361G>A | CA3538753 | IL12B | c.12C>T (p.Ala4=) c.*137C>T (n.*137C>T) c.642C>T (p.Ala214=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.159320361G>C | CA447510880 | IL12B | c.12C>G (p.Ala4=) c.*137C>G (n.*137C>G) c.642C>G (p.Ala214=) | |
5 | g.159320361G= | CA1595017268 | IL12B | c.12C= (p.Ala4=) c.*137C= (n.*137C=) c.642C= (p.Ala214=) | |
5 | g.159320361G>T | CA447510879 | IL12B | c.12C>A (p.Ala4=) c.*137C>A (n.*137C>A) c.642C>A (p.Ala214=) | |
5 | g.159320362G>A | CA3538754 | IL12B | c.11C>T (p.Ala4Val) c.*136C>T (n.*136C>T) c.641C>T (p.Ala214Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.159320362G>C | CA362032498 | IL12B | c.11C>G (p.Ala4Gly) c.*136C>G (n.*136C>G) c.641C>G (p.Ala214Gly) | |
5 | g.159320362G= | CA1595017269 | IL12B | c.11C= (p.Ala4=) c.*136C= (n.*136C=) c.641C= (p.Ala214=) | |
5 | g.159320362G>T | CA362032501 | IL12B | c.11C>A (p.Ala4Asp) c.*136C>A (n.*136C>A) c.641C>A (p.Ala214Asp) | |
5 | g.159320363C>A | CA362032503 | IL12B | c.10G>T (p.Ala4Ser) c.*135G>T (n.*135G>T) c.640G>T (p.Ala214Ser) | |
5 | g.159320363C>G | CA362032505 | IL12B | c.10G>C (p.Ala4Pro) c.*135G>C (n.*135G>C) c.640G>C (p.Ala214Pro) | |
5 | g.159320363C>T | CA362032507 | IL12B | c.10G>A (p.Ala4Thr) c.*135G>A (n.*135G>A) c.640G>A (p.Ala214Thr) | |
5 | g.159320364A= | CA1595017270 | IL12B | c.9T= (p.Asp3=) c.*134T= (n.*134T=) c.639T= (p.Asp213=) | |
5 | g.159320364A>C | CA362032509 | IL12B | c.9T>G (p.Asp3Glu) c.*134T>G (n.*134T>G) c.639T>G (p.Asp213Glu) | |
5 | g.159320364A>G | CA447510889 | IL12B | c.9T>C (p.Asp3=) c.*134T>C (n.*134T>C) c.639T>C (p.Asp213=) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.159320364A>T | CA362032511 | IL12B | c.9T>A (p.Asp3Glu) c.*134T>A (n.*134T>A) c.639T>A (p.Asp213Glu) | gnomAD v3 gnomAD v4 |
5 | g.159320365T>A | CA362032513 | IL12B | c.8A>T (p.Asp3Val) c.*133A>T (n.*133A>T) c.638A>T (p.Asp213Val) | |
5 | g.159320365T>C | CA362032514 | IL12B | c.8A>G (p.Asp3Gly) c.*133A>G (n.*133A>G) c.638A>G (p.Asp213Gly) | |
5 | g.159320365T>G | CA362032516 | IL12B | c.8A>C (p.Asp3Ala) c.*133A>C (n.*133A>C) c.638A>C (p.Asp213Ala) | |
5 | g.159320366C>A | CA362032518 | IL12B | c.7G>T (p.Asp3Tyr) c.*132G>T (n.*132G>T) c.637G>T (p.Asp213Tyr) | |
5 | g.159320366C= | CA1595017271 | IL12B | c.7G= (p.Asp3=) c.*132G= (n.*132G=) c.637G= (p.Asp213=) | |
5 | g.159320366C>G | CA362032519 | IL12B | c.7G>C (p.Asp3His) c.*132G>C (n.*132G>C) c.637G>C (p.Asp213His) | |
5 | g.159320366C>T | CA362032520 | IL12B | c.7G>A (p.Asp3Asn) c.*132G>A (n.*132G>A) c.637G>A (p.Asp213Asn) | dbSNP |
5 | g.159320367C>A | CA447510896 | IL12B | c.6G>T (p.Val2=) c.*131G>T (n.*131G>T) c.636G>T (p.Val212=) | |
5 | g.159320367C>G | CA447510897 | IL12B | c.6G>C (p.Val2=) c.*131G>C (n.*131G>C) c.636G>C (p.Val212=) | |
5 | g.159320367C>T | CA447510899 | IL12B | c.6G>A (p.Val2=) c.*131G>A (n.*131G>A) c.636G>A (p.Val212=) | |
5 | g.159320368A>C | CA362032528 | IL12B | c.5T>G (p.Val2Gly) c.*130T>G (n.*130T>G) c.635T>G (p.Val212Gly) | |
5 | g.159320368A>G | CA362032530 | IL12B | c.5T>C (p.Val2Ala) c.*130T>C (n.*130T>C) c.635T>C (p.Val212Ala) | |
5 | g.159320368A>T | CA362032522 | IL12B | c.5T>A (p.Val2Glu) c.*130T>A (n.*130T>A) c.635T>A (p.Val212Glu) | |
5 | g.159320369C>A | CA362032534 | IL12B | c.4G>T (p.Val2Leu) c.*129G>T (n.*129G>T) c.634G>T (p.Val212Leu) | |
5 | g.159320369C= | CA1595017272 | IL12B | c.4G= (p.Val2=) c.*129G= (n.*129G=) c.634G= (p.Val212=) | |
5 | g.159320369C>G | CA362032532 | IL12B | c.4G>C (p.Val2Leu) c.*129G>C (n.*129G>C) c.634G>C (p.Val212Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
5 | g.159320369C>T | CA362032535 | IL12B | c.4G>A (p.Val2Met) c.*129G>A (n.*129G>A) c.634G>A (p.Val212Met) | dbSNP gnomAD v4 COSMIC COSMIC |
5 | g.159320370C>A | CA362032536 | IL12B | c.3G>T (p.Met1Ile) c.*128G>T (n.*128G>T) c.633G>T (p.Met211Ile) | |
5 | g.159320370C>G | CA362032537 | IL12B | c.3G>C (p.Met1Ile) c.*128G>C (n.*128G>C) c.633G>C (p.Met211Ile) | |
5 | g.159320370C>T | CA362032539 | IL12B | c.3G>A (p.Met1Ile) c.*128G>A (n.*128G>A) c.633G>A (p.Met211Ile) | ClinVar dbSNP gnomAD v4 |
5 | g.159320371A= | CA1595017273 | IL12B | c.2T= (p.Met1=) c.*127T= (n.*127T=) c.632T= (p.Met211=) | |
5 | g.159320371A>C | CA362032544 | IL12B | c.2T>G (p.Met1Arg) c.*127T>G (n.*127T>G) c.632T>G (p.Met211Arg) |