| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.3256546G>C | CA91448392 | MSANTD1 | c.*581G>C (p.=) c.729+689G>C (p.=) n.753+689G>C c.765+653G>C (p.=) | dbSNP |
| 4 | g.3256559C>A | CA91448395 | MSANTD1 | c.*594C>A (p.=) c.729+702C>A (p.=) n.753+702C>A c.765+666C>A (p.=) | dbSNP gnomAD |
| 4 | g.3256560C>T | CA91448404 | MSANTD1 | c.*595C>T (p.=) c.729+703C>T (p.=) n.753+703C>T c.765+667C>T (p.=) | dbSNP |
| 4 | g.3256562C>T | CA91448424 | MSANTD1 | c.*597C>T (p.=) c.729+705C>T (p.=) n.753+705C>T c.765+669C>T (p.=) | dbSNP |
| 4 | g.3256565C>A | CA794017858 | MSANTD1 | c.*600C>A (p.=) c.729+708C>A (p.=) n.753+708C>A c.765+672C>A (p.=) | |
| 4 | g.3256565C>T | CA91448446 | MSANTD1 | c.*600C>T (p.=) c.729+708C>T (p.=) n.753+708C>T c.765+672C>T (p.=) | dbSNP gnomAD |
| 4 | g.3256568C>T | CA549307480 | MSANTD1 | c.*603C>T (p.=) c.729+711C>T (p.=) n.753+711C>T c.765+675C>T (p.=) | gnomAD |
| 4 | g.3256576A>G | CA549307481 | MSANTD1 | c.*611A>G (p.=) c.729+719A>G (p.=) n.753+719A>G c.765+683A>G (p.=) | gnomAD |
| 4 | g.3256579A>C | CA549307482 | MSANTD1 | c.*614A>C (p.=) c.729+722A>C (p.=) n.753+722A>C c.765+686A>C (p.=) | gnomAD |
| 4 | g.3256579A>G | CA91448451 | MSANTD1 | c.*614A>G (p.=) c.729+722A>G (p.=) n.753+722A>G c.765+686A>G (p.=) | dbSNP |
| 4 | g.3256582C>A | CA91448453 | MSANTD1 | c.*617C>A (p.=) c.729+725C>A (p.=) n.753+725C>A c.765+689C>A (p.=) | dbSNP gnomAD |
| 4 | g.3256584A>T | CA91448475 | MSANTD1 | c.*619A>T (p.=) c.729+727A>T (p.=) n.753+727A>T c.765+691A>T (p.=) | dbSNP |
| 4 | g.3256591G>A | CA549307483 | MSANTD1 | c.*626G>A (p.=) c.729+734G>A (p.=) n.753+734G>A c.765+698G>A (p.=) | gnomAD |
| 4 | g.3256594G>A | CA91448477 | MSANTD1 | c.*629G>A (p.=) c.729+737G>A (p.=) n.753+737G>A c.765+701G>A (p.=) | dbSNP gnomAD |
| 4 | g.3256595dup | CA549307484 | MSANTD1 | c.*630dup (p.=) c.729+738dup (p.=) n.753+738dup c.765+702dup (p.=) | gnomAD |
| 4 | g.3256606_3256623del | CA794017885 | MSANTD1 | c.729+749_729+766del (p.=) n.753+749_753+766del c.765+713_765+730del (p.=) | |
| 4 | g.3256609A>G | CA91448478 | MSANTD1 | c.*644A>G (p.=) c.729+752A>G (p.=) n.753+752A>G c.765+716A>G (p.=) | dbSNP gnomAD |
| 4 | g.3256610T>C | CA91448479 | MSANTD1 | c.*645T>C (p.=) c.729+753T>C (p.=) n.753+753T>C c.765+717T>C (p.=) | dbSNP |
| 4 | g.3256614C>A | CA794017899 | MSANTD1 | c.*649C>A (p.=) c.729+757C>A (p.=) n.753+757C>A c.765+721C>A (p.=) | |
| 4 | g.3256614C>T | CA794017894 | MSANTD1 | c.*649C>T (p.=) c.729+757C>T (p.=) n.753+757C>T c.765+721C>T (p.=) | |
| 4 | g.3256615A>G | CA91448480 | MSANTD1 | c.*650A>G (p.=) c.729+758A>G (p.=) n.753+758A>G c.765+722A>G (p.=) | dbSNP |
| 4 | g.3256616G>A | CA794017902 | MSANTD1 | c.729+759G>A (p.=) n.753+759G>A c.765+723G>A (p.=) | |
| 4 | g.3256618C>G | CA91448483 | MSANTD1 | c.729+761C>G (p.=) n.753+761C>G c.765+725C>G (p.=) | dbSNP |
| 4 | g.3256629T>A | CA794017908 | MSANTD1 | c.729+772T>A (p.=) n.753+772T>A c.765+736T>A (p.=) | |
| 4 | g.3256638C>T | CA91448496 | MSANTD1 | c.729+781C>T (p.=) n.753+781C>T c.765+745C>T (p.=) | dbSNP gnomAD |
| 4 | g.3256639T>C | CA91448504 | MSANTD1 | c.729+782T>C (p.=) n.753+782T>C c.765+746T>C (p.=) | dbSNP |
| 4 | g.3256639T>G | CA794017910 | MSANTD1 | c.729+782T>G (p.=) n.753+782T>G c.765+746T>G (p.=) | |
| 4 | g.3256641G>A | CA549307485 | MSANTD1 | c.729+784G>A (p.=) n.753+784G>A c.765+748G>A (p.=) | gnomAD |
| 4 | g.3256646A>G | CA11632806 | MSANTD1 | c.729+789A>G (p.=) n.753+789A>G c.765+753A>G (p.=) | dbSNP gnomAD |
| 4 | g.3256648_3256650del | CA794017915 | MSANTD1 | c.729+791_729+793del (p.=) n.753+791_753+793del c.765+755_765+757del (p.=) |