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Summary

Isoform:
Position:
429
Ref:
G
Mutation:
C
PTM impact:
proximal
PTM affected:
3
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

[0.0199681]

PTM Site: 425S

Affected site:

Position: 425
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
431Q TPGSDVDSVGGGS[E/Q]ES 6
distal
426M TPGSDVDS[V/M]VGGGSES 1
proximal
419L T[P/L]PGSDVDSVGGGSES 6
distal
429C TPGSDVDSVGG[G/C]GSES 4
distal

PTM Site: 430S

Affected site:

Position: 430
Residue: S
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
433W VDSVGGGSES[R/W]RSLDS 3
distal
432C VDSVGGGSE[S/C]SRSLDS 2
proximal
431Q VDSVGGGS[E/Q]ESRSLDS 1
proximal
426M VDS[V/M]VGGGSESRSLDS 4
distal
436N VDSVGGGSESRSL[D/N]DS 6
distal
429C VDSVGG[G/C]GSESRSLDS 1
proximal

PTM Site: 434S

Affected site:

Position: 434
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
433W GGGSES[R/W]RSLDSPTSS 1
proximal
432C GGGSE[S/C]SRSLDSPTSS 2
proximal
431Q GGGS[E/Q]ESRSLDSPTSS 3
distal
436N GGGSESRSL[D/N]DSPTSS 2
network-rewiring
429C GG[G/C]GSESRSLDSPTSS 5
distal
437A GGGSESRSLD[S/A]SPTSS 3
network-rewiring
440F GGGSESRSLDSPT[S/F]SS 6
distal

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