| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.157198907G>T | CA452784000 | ARID1B | c.4320G>T (p.Pro1440=) c.4389G>T (p.Pro1463=) c.4608G>T (p.Pro1536=) c.4359G>T (p.Pro1453=) c.4071G>T (p.Pro1357=) c.2637G>T (p.Pro879=) c.1800G>T (p.Pro600=) c.1431G>T (p.Pro477=) n.2942G>T n.399G>T c.4479G>T (p.Pro1493=) n.2476G>T c.1847G>T c.1761G>T n.1145G>T c.1821G>T (p.Pro607=) c.1980G>T (p.Pro660=) c.4110G>T (p.Pro1370=) c.4230G>T (p.Pro1410=) c.3309G>T (p.Pro1103=) c.3129G>T (p.Pro1043=) c.2889G>T (p.Pro963=) c.2508G>T (p.Pro836=) c.1371G>T (p.Pro457=) c.4440G>T (p.Pro1480=) c.4341G>T (p.Pro1447=) c.4311G>T (p.Pro1437=) c.4281G>T (p.Pro1427=) c.4152G>T (p.Pro1384=) c.4131G>T (p.Pro1377=) n.4427-1798G>T | dbSNP gnomAD v4 |
| 6 | g.157198907G>C | CA452783999 | ARID1B | c.4320G>C (p.Pro1440=) c.4389G>C (p.Pro1463=) c.4608G>C (p.Pro1536=) c.4359G>C (p.Pro1453=) c.4071G>C (p.Pro1357=) c.2637G>C (p.Pro879=) c.1800G>C (p.Pro600=) c.1431G>C (p.Pro477=) n.2942G>C n.399G>C c.4479G>C (p.Pro1493=) n.2476G>C c.1847G>C c.1761G>C n.1145G>C c.1821G>C (p.Pro607=) c.1980G>C (p.Pro660=) c.4110G>C (p.Pro1370=) c.4230G>C (p.Pro1410=) c.3309G>C (p.Pro1103=) c.3129G>C (p.Pro1043=) c.2889G>C (p.Pro963=) c.2508G>C (p.Pro836=) c.1371G>C (p.Pro457=) c.4440G>C (p.Pro1480=) c.4341G>C (p.Pro1447=) c.4311G>C (p.Pro1437=) c.4281G>C (p.Pro1427=) c.4152G>C (p.Pro1384=) c.4131G>C (p.Pro1377=) n.4427-1798G>C | ClinVar dbSNP COSMIC COSMIC |
| 6 | g.157198907G>A | CA207808 | ARID1B | c.4320G>A (p.Pro1440=) c.4389G>A (p.Pro1463=) c.4608G>A (p.Pro1536=) c.4359G>A (p.Pro1453=) c.4071G>A (p.Pro1357=) c.2637G>A (p.Pro879=) c.1800G>A (p.Pro600=) c.1431G>A (p.Pro477=) n.2942G>A n.399G>A c.4479G>A (p.Pro1493=) n.2476G>A c.1847G>A c.1761G>A n.1145G>A c.1821G>A (p.Pro607=) c.1980G>A (p.Pro660=) c.4110G>A (p.Pro1370=) c.4230G>A (p.Pro1410=) c.3309G>A (p.Pro1103=) c.3129G>A (p.Pro1043=) c.2889G>A (p.Pro963=) c.2508G>A (p.Pro836=) c.1371G>A (p.Pro457=) c.4440G>A (p.Pro1480=) c.4341G>A (p.Pro1447=) c.4311G>A (p.Pro1437=) c.4281G>A (p.Pro1427=) c.4152G>A (p.Pro1384=) c.4131G>A (p.Pro1377=) n.4427-1798G>A | ClinVar dbSNP gnomAD v4 |