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Mutation:
STARD13 T57M
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.2691]
Minor Allele Frequency: (1000 Genomes)
[3.1349799999999997]
PTM Site: 53S
Affected site:
Position: 53
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 57M | PRGDRNGSPGG[T/M]TGMR | 4 |
distal
|
| 51S | PRGDR[N/S]NGSPGGTGMR | 2 |
proximal
|
| 54L | PRGDRNGS[P/L]PGGTGMR | 1 |
network-rewiring
|
| 53L | PRGDRNG[S/L]SPGGTGMR | 0 |
direct
|
| 52V | PRGDRN[G/V]GSPGGTGMR | 1 |
proximal
|
| 47Q | P[R/Q]RGDRNGSPGGTGMR | 6 |
distal
|
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