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Mutation:
CRACR2A R53G
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
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: 54K
Affected site:
Position: 54
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
53G | GQLVML[R/G]RKAQEFFQT | 1 |
proximal
|
54N | GQLVMLR[K/N]KAQEFFQT | 0 |
direct
|
56L | GQLVMLRKA[Q/L]QEFFQT | 2 |
proximal
|
55S | GQLVMLRK[A/S]AQEFFQT | 1 |
proximal
|
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