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Summary

Isoform:
Position:
313
Ref:
T
Mutation:
K
PTM impact:
direct
PTM affected:
1
Kinases:

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: 313T

Affected site:

Position: 313
Residue: T
Type: phosphorylation

Impact:

direct

Other known mutations affecting this site

Mutation In sequence Distance Impact
315Y SSFQKERTD[D/Y]DEQFAD 2
network-rewiring
313K SSFQKER[T/K]TDDEQFAD 0
direct
309H SSF[Q/H]QKERTDDEQFAD 4
distal
319T SSFQKERTDDEQF[A/T]AD 6
distal
311Q SSFQK[E/Q]ERTDDEQFAD 2
network-rewiring
314N SSFQKERT[D/N]DDEQFAD 1
proximal
314G SSFQKERT[D/G]DDEQFAD 1
proximal

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