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Mutation:
FOLH1 N121S
Summary
Clinical Information
Cancer types: (TCGA MC3)
BRCA
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0077]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 121N
Affected site:
Position: 121
Residue: N
Type: N-glycosylation, glycosylation
Impact:
directOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 121S | DVLLSYP[N/S]NKTHPNYI | 0 |
direct
|
| 115A | D[V/A]VLLSYPNKTHPNYI | 6 |
distal
|
| 125S | DVLLSYPNKTH[P/S]PNYI | 4 |
distal
|
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