| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.49913503C>A | CA412080274 | ALG12 | c.177G>T (p.Glu59Asp) | |
| 22 | g.49913503C= | CA2410564775 | ALG12 | c.177G= (p.Glu59=) | |
| 22 | g.49913503C>G | CA412080276 | ALG12 | c.177G>C (p.Glu59Asp) | |
| 22 | g.49913503C>T | CA10300707 | ALG12 | c.177G>A (p.Glu59=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 22 | g.49913504T>A | CA412080283 | ALG12 | c.176A>T (p.Glu59Val) | |
| 22 | g.49913504T>C | CA412080292 | ALG12 | c.176A>G (p.Glu59Gly) | |
| 22 | g.49913504T>G | CA412080295 | ALG12 | c.176A>C (p.Glu59Ala) | dbSNP gnomAD v4 |
| 22 | g.49913504T= | CA2410564776 | ALG12 | c.176A= (p.Glu59=) | |
| 22 | g.49913505C>A | CA412080298 | ALG12 | c.175G>T (p.Glu59Ter) | |
| 22 | g.49913505C>G | CA412080307 | ALG12 | c.175G>C (p.Glu59Gln) | ClinVar gnomAD v4 |
| 22 | g.49913505C>T | CA412080304 | ALG12 | c.175G>A (p.Glu59Lys) | |
| 22 | g.49913506A>C | CA515106783 | ALG12 | c.174T>G (p.Leu58=) | |
| 22 | g.49913506A>G | CA515106785 | ALG12 | c.174T>C (p.Leu58=) | gnomAD v4 COSMIC |
| 22 | g.49913506A>T | CA515106787 | ALG12 | c.174T>A (p.Leu58=) | |
| 22 | g.49913507A>C | CA412080311 | ALG12 | c.173T>G (p.Leu58Arg) | |
| 22 | g.49913507A>G | CA412080313 | ALG12 | c.173T>C (p.Leu58Pro) | |
| 22 | g.49913507A>T | CA412080314 | ALG12 | c.173T>A (p.Leu58His) | |
| 22 | g.49913508G>A | CA412080316 | ALG12 | c.172C>T (p.Leu58Phe) | |
| 22 | g.49913508G>C | CA412080319 | ALG12 | c.172C>G (p.Leu58Val) | |
| 22 | g.49913508G>T | CA412080323 | ALG12 | c.172C>A (p.Leu58Ile) | |
| 22 | g.49913509A>C | CA412080332 | ALG12 | c.171T>G (p.His57Gln) | |
| 22 | g.49913509A>G | CA515106790 | ALG12 | c.171T>C (p.His57=) | |
| 22 | g.49913509A>T | CA412080335 | ALG12 | c.171T>A (p.His57Gln) | |
| 22 | g.49913510T>A | CA412080336 | ALG12 | c.170A>T (p.His57Leu) | dbSNP |
| 22 | g.49913510T>C | CA412080337 | ALG12 | c.170A>G (p.His57Arg) | |
| 22 | g.49913510T>G | CA412080338 | ALG12 | c.170A>C (p.His57Pro) | |
| 22 | g.49913510T= | CA2410564777 | ALG12 | c.170A= (p.His57=) | |
| 22 | g.49913511G>A | CA412080341 | ALG12 | c.169C>T (p.His57Tyr) | |
| 22 | g.49913511G>C | CA412080350 | ALG12 | c.169C>G (p.His57Asp) | |
| 22 | g.49913511G>T | CA412080344 | ALG12 | c.169C>A (p.His57Asn) | COSMIC |
| 22 | g.49913512G>A | CA515106793 | ALG12 | c.168C>T (p.Asp56=) | ClinVar |
| 22 | g.49913512G>C | CA412080354 | ALG12 | c.168C>G (p.Asp56Glu) | gnomAD v4 |
| 22 | g.49913512G>T | CA412080356 | ALG12 | c.168C>A (p.Asp56Glu) | |
| 22 | g.49913513T>A | CA412080358 | ALG12 | c.167A>T (p.Asp56Val) | |
| 22 | g.49913513T>C | CA412080360 | ALG12 | c.167A>G (p.Asp56Gly) | |
| 22 | g.49913513T>G | CA412080361 | ALG12 | c.167A>C (p.Asp56Ala) | |
| 22 | g.49913514C>A | CA412080366 | ALG12 | c.166G>T (p.Asp56Tyr) | gnomAD v4 |
| 22 | g.49913514C= | CA2410564778 | ALG12 | c.166G= (p.Asp56=) | |
| 22 | g.49913514C>G | CA412080367 | ALG12 | c.166G>C (p.Asp56His) | |
| 22 | g.49913514C>T | CA10300708 | ALG12 | c.166G>A (p.Asp56Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.49913515G>A | CA10300709 | ALG12 | c.165C>T (p.Tyr55=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 22 | g.49913515G>C | CA412080377 | ALG12 | c.165C>G (p.Tyr55Ter) | |
| 22 | g.49913515G= | CA2410564779 | ALG12 | c.165C= (p.Tyr55=) | |
| 22 | g.49913515G>T | CA412080385 | ALG12 | c.165C>A (p.Tyr55Ter) | ClinVar dbSNP |
| 22 | g.49913516T>A | CA412080390 | ALG12 | c.164A>T (p.Tyr55Phe) | |
| 22 | g.49913516T>C | CA412080394 | ALG12 | c.164A>G (p.Tyr55Cys) | |
| 22 | g.49913516T>G | CA412080395 | ALG12 | c.164A>C (p.Tyr55Ser) | |
| 22 | g.49913517A>C | CA412080397 | ALG12 | c.163T>G (p.Tyr55Asp) | |
| 22 | g.49913517A>G | CA412080400 | ALG12 | c.163T>C (p.Tyr55His) | |
| 22 | g.49913517A>T | CA412080396 | ALG12 | c.163T>A (p.Tyr55Asn) |