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Mutation:
CLEC16A R443H
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0081]
Minor Allele Frequency: (1000 Genomes)
[0.0199681]
PTM Site: 445K
Affected site:
Position: 445
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 443H | MVIME[R/H]RSKLSELAAS | 2 |
proximal
|
| 451T | MVIMERSKLSELA[A/T]AS | 6 |
distal
|
| 451G | MVIMERSKLSELA[A/G]AS | 6 |
distal
|
| 447L | MVIMERSKL[S/L]SELAAS | 2 |
proximal
|
| 450V | MVIMERSKLSEL[A/V]AAS | 5 |
distal
|
| 444N | MVIMER[S/N]SKLSELAAS | 1 |
proximal
|
| 444R | MVIMER[S/R]SKLSELAAS | 1 |
proximal
|
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