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Summary

Isoform:
Position:
172
Ref:
N
Mutation:
D
PTM impact:
proximal
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: 170T

Affected site:

Position: 170
Residue: T
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
176I LGNVLTSTPNAKT[V/I]VN 6
distal
172D LGNVLTSTP[N/D]NAKTVN 2
proximal
171L LGNVLTST[P/L]PNAKTVN 1
network-rewiring
173T LGNVLTSTPN[A/T]AKTVN 3
distal
168I LGNVL[T/I]TSTPNAKTVN 2
proximal
176F LGNVLTSTPNAKT[V/F]VN 6
distal

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