[SOCS1]
Mutation tier
| Entity | Tier | Description |
|---|---|---|
| BL | 2 | relevance in BL not firmly established |
| DLBCL | 1 | high-confidence DLBCL gene |
| FL | 1 | high-confidence FL gene |
Mutation incidence
| Entity | source | frequency (%) |
|---|---|---|
| BL | GAMBL genomes+capture | 1.85 |
| BL | Thomas cohort | 1.70 |
| BL | Panea cohort | 3.00 |
| DLBCL | GAMBL genomes | 15.30 |
| DLBCL | Schmitz cohort | 12.80 |
| DLBCL | Reddy cohort | 10.40 |
| DLBCL | Chapuy cohort | 4.70 |
| FL | GAMBL genomes | 9.70 |
Mutation pattern
| Entity | aSHM | Significant selection | dN/dS (missense) | dN/dS (nonsense) |
|---|---|---|---|---|
| BL | Yes | No | 4.476 | 0.000 |
| DLBCL | Yes | Yes | 5.023 | 17.509 |
| FL | Yes | Yes | 21.460 | 123.344 |
aSHM regions
| chr_name | hg19_start | hg19_end | region | regulatory_comment |
|---|---|---|---|---|
| chr16 | 11347512 | 11350007 | intron-1 | enhancer |
## SOCS1 Hotspots
| Chromosome | Coordinate (hg19) | ref>alt | HGVSp |
|---|---|---|---|
| chr16 | 11349022 | T>C | D105G |
| chr16 | 11349019 | C>T | S106N |
| chr16 | 11349018 | G>C | S106R |
| chr16 | 11349006 | G>C | N110K |
| chr16 | 11349004 | C>T | C111Y |
| chr16 | 11349004 | C>G | C111S |
| chr16 | 11349003 | G>C | C111W |
| chr16 | 11349001 | A>T | F112Y |
| chr16 | 11348989 | C>T | S116N |
| chr16 | 11348988 | G>C | S116R |
| chr16 | 11348987 | C>T | V117M |
| chr16 | 11348981 | T>C | M119V |
| chr16 | 11348980 | A>T | M119K |
| chr16 | 11348977 | G>C | A120G |
| chr16 | 11348972 | C>T | G122R |
| chr16 | 11348972 | C>A | G122* |
| chr16 | 11348969 | G>A | P123S |
| chr16 | 11348962 | C>G | S125T |
| chr16 | 11348956 | C>T | R127H |
| chr16 | 11348951 | G>T | H129N |
| chr16 | 11348951 | G>A | H129Y |
| chr16 | 11348945 | G>A | Q131* |
| chr16 | 11348936 | G>A | R134C |
| chr16 | 11348933 | A>G | F135L |
| chr16 | 11348932 | A>C | F135C |
View coding variants in ProteinPaint hg19 or hg38
View all variants in GenomePaint hg19 or hg38


