| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.7676335_7676366del | CA913187845 | TP53 | c.96+25_97-54del (n.96+25_97-54del) c.-21-1121_-21-1090del (n.-21-1121_-21-1090del) c.96+25_96+56del (n.96+25_96+56del) n.352+25_353-54del c.-22+25_-21-54del (n.-22+25_-21-54del) | ClinVar dbSNP |
| 17 | g.7676351_7676366del | CA000510 | TP53 | c.96+41_97-54del (n.96+41_97-54del) c.-21-1105_-21-1090del (n.-21-1105_-21-1090del) c.96+41_96+56del (n.96+41_96+56del) n.352+41_353-54del c.-22+41_-21-54del (n.-22+41_-21-54del) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.7676351_7676366dup | CA658683995 | TP53 | c.96+41_97-54dup (n.96+41_97-54dup) c.-21-1105_-21-1090dup (n.-21-1105_-21-1090dup) c.96+41_96+56dup (n.96+41_96+56dup) n.352+41_353-54dup c.-22+41_-21-54dup (n.-22+41_-21-54dup) | ClinVar dbSNP gnomAD v4 |