| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.85756967G>A | CA15842826 | LINC02883 | n.419+917C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.85756967G= | CA2192802077 | LINC02883 | n.419+917C= | |
| 15 | g.85756968C>A | CA619465434 | LINC02883 | n.419+916G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.85756968C= | CA2192802083 | LINC02883 | n.419+916G= | |
| 15 | g.85756968C>T | CA2192802085 | LINC02883 | n.419+916G>A | dbSNP |
| 15 | g.85756969T>G | CA716533392 | LINC02883 | n.419+915A>C | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.85756969T= | CA2192802087 | LINC02883 | n.419+915A= | |
| 15 | g.85756970G= | CA2192802090 | LINC02883 | n.419+914C= | |
| 15 | g.85756970G>T | CA716533396 | LINC02883 | n.419+914C>A | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.85756975G>A | CA274415627 | LINC02883 | n.419+909C>T | dbSNP |
| 15 | g.85756975G= | CA2192802094 | LINC02883 | n.419+909C= | |
| 15 | g.85756977C= | CA2192802100 | LINC02883 | n.419+907G= | |
| 15 | g.85756977C>T | CA274415631 | LINC02883 | n.419+907G>A | dbSNP |
| 15 | g.85756980G>A | CA274415639 | LINC02883 | n.419+904C>T | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.85756980G= | CA2192802111 | LINC02883 | n.419+904C= | |
| 15 | g.85756980_85757002delinsGTGGAGGAGGCAGTTGGCTACCC | CA2192802113 | LINC02883 | n.419+882_419+904delinsGGGTAGCCAACTGCCTCCTCCAC | |
| 15 | g.85756982_85757003del | CA716533412 | LINC02883 | n.419+882_419+903del | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.85756982G>A | CA2192802119 | LINC02883 | n.419+902C>T | dbSNP |
| 15 | g.85756982G= | CA2192802117 | LINC02883 | n.419+902C= | |
| 15 | g.85756983G>A | CA274415646 | LINC02883 | n.419+901C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.85756983G= | CA2192802121 | LINC02883 | n.419+901C= | |
| 15 | g.85756984A>C | CA2563261120 | LINC02883 | n.419+900T>G | |
| 15 | g.85756985G>A | CA2192802125 | LINC02883 | n.419+899C>T | dbSNP |
| 15 | g.85756985G= | CA2192802123 | LINC02883 | n.419+899C= | |
| 15 | g.85756986G>C | CA2192802128 | LINC02883 | n.419+898C>G | dbSNP |
| 15 | g.85756986G= | CA2192802127 | LINC02883 | n.419+898C= | |
| 15 | g.85756987A= | CA2192802132 | LINC02883 | n.419+897T= | |
| 15 | g.85756987A>C | CA274415650 | LINC02883 | n.419+897T>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.85756993T>C | CA2192802136 | LINC02883 | n.419+891A>G | dbSNP |
| 15 | g.85756993T= | CA2192802134 | LINC02883 | n.419+891A= | |
| 15 | g.85756997C= | CA2192802141 | LINC02883 | n.419+887G= | |
| 15 | g.85756997C>T | CA274415655 | LINC02883 | n.419+887G>A | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.85757000C>A | CA716533429 | LINC02883 | n.419+884G>T | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.85757000C= | CA2192802146 | LINC02883 | n.419+884G= | |
| 15 | g.85757004C>A | CA716533431 | LINC02883 | n.419+880G>T | dbSNP |
| 15 | g.85757004C= | CA2192802148 | LINC02883 | n.419+880G= | |
| 15 | g.85757004_85757082delinsCTCCTTGCCCTTGGCAACTTGACAGTCCCCCCAGGCAGGCTCTCAGGATGCCAAAGCCTCCAAGATGGCCCGTTTTCTT | CA2192802151 | LINC02883 | n.419+802_419+880delinsAAGAAAACGGGCCATCTTGGAGGCTTTGGCATCCTGAGAGCCTGCCTGGGGGGACTGTCAAGTTGCCAAGGGCAAGGAG | |
| 15 | g.85757005T>G | CA2192802157 | LINC02883 | n.419+879A>C | dbSNP |
| 15 | g.85757005T= | CA2192802155 | LINC02883 | n.419+879A= | |
| 15 | g.85757009_85757086del | CA972306153 | LINC02883 | n.419+802_419+879del | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.85757006C= | CA2192802159 | LINC02883 | n.419+878G= | |
| 15 | g.85757006C>T | CA972306171 | LINC02883 | n.419+878G>A | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.85757007C= | CA2192802161 | LINC02883 | n.419+877G= | |
| 15 | g.85757007C>G | CA2192802162 | LINC02883 | n.419+877G>C | dbSNP |
| 15 | g.85757009T>C | CA716533432 | LINC02883 | n.419+875A>G | dbSNP |
| 15 | g.85757009T= | CA2192802164 | LINC02883 | n.419+875A= | |
| 15 | g.85757011C= | CA2192802171 | LINC02883 | n.419+873G= | |
| 15 | g.85757011C>T | CA619465435 | LINC02883 | n.419+873G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.85757012C= | CA2192802173 | LINC02883 | n.419+872G= | |
| 15 | g.85757012C>G | CA2192802175 | LINC02883 | n.419+872G>C | dbSNP |