Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.74192332G>A | CA2046626498 | LINC02882 | n.553+1742C>T | dbSNP |
12 | g.74192332G= | CA2046626497 | LINC02882 | n.553+1742C= | |
12 | g.74192332G>T | CA2046626499 | LINC02882 | n.553+1742C>A | dbSNP |
12 | g.74192336T>C | CA2516311819 | LINC02882 | n.553+1738A>G | |
12 | g.74192337G>A | CA239777136 | LINC02882 | n.553+1737C>T | dbSNP |
12 | g.74192337G= | CA2046626500 | LINC02882 | n.553+1737C= | |
12 | g.74192339C>T | CA2515247546 | LINC02882 | n.553+1735G>A | |
12 | g.74192343T>C | CA239777137 | LINC02882 | n.553+1731A>G | dbSNP gnomAD v3 gnomAD v4 |
12 | g.74192343T= | CA2046626501 | LINC02882 | n.553+1731A= | |
12 | g.74192345C>A | CA691780364 | LINC02882 | n.553+1729G>T | dbSNP gnomAD v3 gnomAD v4 |
12 | g.74192345C= | CA2046626503 | LINC02882 | n.553+1729G= | |
12 | g.74192345C>T | CA239777138 | LINC02882 | n.553+1729G>A | dbSNP gnomAD v3 gnomAD v4 |
12 | g.74192347T>A | CA691780369 | LINC02882 | n.553+1727A>T | dbSNP gnomAD v3 gnomAD v4 |
12 | g.74192347T= | CA2046626505 | LINC02882 | n.553+1727A= | |
12 | g.74192350T>C | CA2726539734 | LINC02882 | n.553+1724A>G | dbSNP |
12 | g.74192352T>C | CA606067090 | LINC02882 | n.553+1722A>G | dbSNP gnomAD v2 |
12 | g.74192352T= | CA2046626507 | LINC02882 | n.553+1722A= | |
12 | g.74192352_74192353insG | CA2568208413 | LINC02882 | n.553+1721_553+1722insC | |
12 | g.74192354G= | CA2046626508 | LINC02882 | n.553+1720C= | |
12 | g.74192354G>T | CA691780371 | LINC02882 | n.553+1720C>A | dbSNP |
12 | g.74192358T>G | CA239777139 | LINC02882 | n.553+1716A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.74192358T= | CA2046626510 | LINC02882 | n.553+1716A= | |
12 | g.74192362T>C | CA691780376 | LINC02882 | n.553+1712A>G | dbSNP |
12 | g.74192362T= | CA2046626513 | LINC02882 | n.553+1712A= | |
12 | g.74192367T>A | CA691780384 | LINC02882 | n.553+1707A>T | dbSNP |
12 | g.74192367T= | CA2046626515 | LINC02882 | n.553+1707A= | |
12 | g.74192372T>C | CA2046626518 | LINC02882 | n.553+1702A>G | dbSNP |
12 | g.74192372T= | CA2046626517 | LINC02882 | n.553+1702A= | |
12 | g.74192373A= | CA2046626520 | LINC02882 | n.553+1701T= | |
12 | g.74192373A>T | CA2046626521 | LINC02882 | n.553+1701T>A | dbSNP |
12 | g.74192374G= | CA2046626523 | LINC02882 | n.553+1700C= | |
12 | g.74192374G>T | CA691780390 | LINC02882 | n.553+1700C>A | dbSNP gnomAD v3 gnomAD v4 |
12 | g.74192378C>A | CA691780393 | LINC02882 | n.553+1696G>T | dbSNP gnomAD v3 gnomAD v4 |
12 | g.74192378C= | CA2046626525 | LINC02882 | n.553+1696G= | |
12 | g.74192380G>C | CA2046626529 | LINC02882 | n.553+1694C>G | dbSNP |
12 | g.74192380G= | CA2046626528 | LINC02882 | n.553+1694C= | |
12 | g.74192381C= | CA2046626531 | LINC02882 | n.553+1693G= | |
12 | g.74192381C>T | CA239777140 | LINC02882 | n.553+1693G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.74192386del | CA2726539735 | LINC02882 | n.553+1691del | dbSNP |
12 | g.74192388A= | CA2046626533 | LINC02882 | n.553+1686T= | |
12 | g.74192388A>G | CA239777141 | LINC02882 | n.553+1686T>C | dbSNP gnomAD v3 gnomAD v4 |
12 | g.74192388A>T | CA691780396 | LINC02882 | n.553+1686T>A | dbSNP gnomAD v3 gnomAD v4 |
12 | g.74192389T>C | CA239777142 | LINC02882 | n.553+1685A>G | dbSNP gnomAD v3 gnomAD v4 |
12 | g.74192389T= | CA2046626535 | LINC02882 | n.553+1685A= | |
12 | g.74192390G>A | CA239777143 | LINC02882 | n.553+1684C>T | dbSNP gnomAD v3 gnomAD v4 |
12 | g.74192390G= | CA2046626537 | LINC02882 | n.553+1684C= | |
12 | g.74192397T>C | CA691780403 | LINC02882 | n.553+1677A>G | dbSNP gnomAD v3 gnomAD v4 |
12 | g.74192397T= | CA2046626541 | LINC02882 | n.553+1677A= | |
12 | g.74192399T>A | CA655038664 | LINC02882 | n.553+1675A>T | COSMIC |
12 | g.74192400A= | CA2046626543 | LINC02882 | n.553+1674T= |