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Summary

Isoform:
Position:
56
Ref:
S
Mutation:
G
PTM impact:
direct
PTM affected:
5
Kinases:
AURKB, AURORA A, AURKB, AURKA, PAK4, SRC

Clinical Information

Cancer types: (TCGA MC3)

LUSC, PAAD, LGG

Cancer types: (PCAWG)

Liver-HCC, Eso-AdenoCa, Panc-AdenoCA

Disease Annotations: (ClinVar)

Li-Fraumeni syndrome, Ovarian Neoplasms, Hereditary cancer-predisposing syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 50R

PTM Site: 52T

Affected site:

Position: 52
Residue: T
Type: phosphorylation

Impact:

distal

PTM Site: 56S

Affected site:

Position: 56
Residue: S
Type: phosphorylation

Impact:

direct

Other known mutations affecting this site

Mutation In sequence Distance Impact
62A DRNTFRHSVVVPY[E/A]EP 6
distal
62K DRNTFRHSVVVPY[E/K]EP 6
distal
61C DRNTFRHSVVVP[Y/C]YEP 5
distal
61S DRNTFRHSVVVP[Y/S]YEP 5
distal
61D DRNTFRHSVVVP[Y/D]YEP 5
distal
61H DRNTFRHSVVVP[Y/H]YEP 5
distal
61N DRNTFRHSVVVP[Y/N]YEP 5
distal
60L DRNTFRHSVVV[P/L]PYEP 4
distal
60R DRNTFRHSVVV[P/R]PYEP 4
distal
60S DRNTFRHSVVV[P/S]PYEP 4
distal
59G DRNTFRHSVV[V/G]VPYEP 3
distal
59M DRNTFRHSVV[V/M]VPYEP 3
distal
58M DRNTFRHSV[V/M]VVPYEP 2
proximal
57G DRNTFRHS[V/G]VVVPYEP 1
proximal
57E DRNTFRHS[V/E]VVVPYEP 1
proximal
57L DRNTFRHS[V/L]VVVPYEP 1
proximal
57M DRNTFRHS[V/M]VVVPYEP 1
proximal
56R DRNTFRH[S/R]SVVVPYEP 0
direct
56I DRNTFRH[S/I]SVVVPYEP 0
direct
56T DRNTFRH[S/T]SVVVPYEP 0
direct
56N DRNTFRH[S/N]SVVVPYEP 0
direct
56G DRNTFRH[S/G]SVVVPYEP 0
direct
55Q DRNTFR[H/Q]HSVVVPYEP 1
proximal
55L DRNTFR[H/L]HSVVVPYEP 1
proximal
55R DRNTFR[H/R]HSVVVPYEP 1
proximal
55P DRNTFR[H/P]HSVVVPYEP 1
proximal
55N DRNTFR[H/N]HSVVVPYEP 1
proximal
54L DRNTF[R/L]RHSVVVPYEP 2
network-rewiring
54P DRNTF[R/P]RHSVVVPYEP 2
network-rewiring
54Q DRNTF[R/Q]RHSVVVPYEP 2
network-rewiring
54G DRNTF[R/G]RHSVVVPYEP 2
network-rewiring
53I DRNT[F/I]FRHSVVVPYEP 3
distal
52A DRN[T/A]TFRHSVVVPYEP 4
distal
52P DRN[T/P]TFRHSVVVPYEP 4
distal
51Y DR[N/Y]NTFRHSVVVPYEP 5
distal
50K D[R/K]RNTFRHSVVVPYEP 6
distal
50G D[R/G]RNTFRHSVVVPYEP 6
distal
52I DRN[T/I]TFRHSVVVPYEP 4
distal
59E DRNTFRHSVV[V/E]VPYEP 3
distal
53V DRNT[F/V]FRHSVVVPYEP 3
distal
58G DRNTFRHSV[V/G]VVPYEP 2
proximal

PTM Site: 61Y

Affected site:

Position: 61
Residue: Y
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
67V RHSVVVPYEPPEV[G/V]GS 6
distal
67A RHSVVVPYEPPEV[G/A]GS 6
distal
67S RHSVVVPYEPPEV[G/S]GS 6
distal
66D RHSVVVPYEPPE[V/D]VGS 5
distal
66I RHSVVVPYEPPE[V/I]VGS 5
distal
65G RHSVVVPYEPP[E/G]EVGS 4
distal
65A RHSVVVPYEPP[E/A]EVGS 4
distal
65K RHSVVVPYEPP[E/K]EVGS 4
distal
64L RHSVVVPYEP[P/L]PEVGS 3
network-rewiring
63L RHSVVVPYE[P/L]PPEVGS 2
proximal
63S RHSVVVPYE[P/S]PPEVGS 2
proximal
62A RHSVVVPY[E/A]EPPEVGS 1
proximal
62K RHSVVVPY[E/K]EPPEVGS 1
proximal
61C RHSVVVP[Y/C]YEPPEVGS 0
direct
61S RHSVVVP[Y/S]YEPPEVGS 0
direct
61D RHSVVVP[Y/D]YEPPEVGS 0
direct
61H RHSVVVP[Y/H]YEPPEVGS 0
direct
61N RHSVVVP[Y/N]YEPPEVGS 0
direct
60L RHSVVV[P/L]PYEPPEVGS 1
proximal
60R RHSVVV[P/R]PYEPPEVGS 1
proximal
60S RHSVVV[P/S]PYEPPEVGS 1
proximal
59G RHSVV[V/G]VPYEPPEVGS 2
proximal
59M RHSVV[V/M]VPYEPPEVGS 2
proximal
58M RHSV[V/M]VVPYEPPEVGS 3
distal
57G RHS[V/G]VVVPYEPPEVGS 4
distal
57E RHS[V/E]VVVPYEPPEVGS 4
distal
57L RHS[V/L]VVVPYEPPEVGS 4
distal
57M RHS[V/M]VVVPYEPPEVGS 4
distal
56R RH[S/R]SVVVPYEPPEVGS 5
distal
56I RH[S/I]SVVVPYEPPEVGS 5
distal
56T RH[S/T]SVVVPYEPPEVGS 5
distal
56N RH[S/N]SVVVPYEPPEVGS 5
distal
56G RH[S/G]SVVVPYEPPEVGS 5
distal
55Q R[H/Q]HSVVVPYEPPEVGS 6
distal
55L R[H/L]HSVVVPYEPPEVGS 6
distal
55R R[H/R]HSVVVPYEPPEVGS 6
distal
55P R[H/P]HSVVVPYEPPEVGS 6
distal
55N R[H/N]HSVVVPYEPPEVGS 6
distal
64H RHSVVVPYEP[P/H]PEVGS 3
network-rewiring
65D RHSVVVPYEPP[E/D]EVGS 4
distal
59E RHSVV[V/E]VPYEPPEVGS 2
proximal
58G RHSV[V/G]VVPYEPPEVGS 3
distal

External references

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