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Mutation:
ECT2L S91F
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.3719]
Minor Allele Frequency: (1000 Genomes)
[0.17971199999999998]
PTM Site: 86S
Affected site:
Position: 86
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
83C | TVLP[R/C]RFISLYIFSFL | 3 |
distal
|
90V | TVLPRFISLYI[F/V]FSFL | 4 |
distal
|
91F | TVLPRFISLYIF[S/F]SFL | 5 |
distal
|
81I | TV[L/I]LPRFISLYIFSFL | 5 |
distal
|
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