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Mutation:
BCL2L12 R143Q
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0231]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 143R
Affected site:
Position: 143
Residue: R
Type: methylation
Impact:
directOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 143Q | CLPCSLG[R/Q]RGAAPSES | 0 |
direct
|
| 148C | CLPCSLGRGAAP[S/C]SES | 5 |
distal
|
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