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Summary

Isoform:
Position:
45
Ref:
G
Mutation:
S
PTM impact:
proximal
PTM affected:
3
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Hereditary nonpolyposis colorectal neoplasms

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 41S

Affected site:

Position: 41
Residue: S
Type: phosphorylation (SARS-CoV-2), phosphorylation

Impact:

distal

Other known mutations affecting this site

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Mutation
In sequence
Distance
Impact
41Y AAAAPGA[S/Y]SPSPGGDA 0
direct
41C AAAAPGA[S/C]SPSPGGDA 0
direct
41F AAAAPGA[S/F]SPSPGGDA 0
direct
40T AAAAPG[A/T]ASPSPGGDA 1
proximal
40P AAAAPG[A/P]ASPSPGGDA 1
proximal
Showing 1 to 5 of 34 rows

PTM Site: 43S

Affected site:

Position: 43
Residue: S
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

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Mutation
In sequence
Distance
Impact
43P AAPGASP[S/P]SPGGDAAW 0
direct
43F AAPGASP[S/F]SPGGDAAW 0
direct
42A AAPGAS[P/A]PSPGGDAAW 1
proximal
42S AAPGAS[P/S]PSPGGDAAW 1
proximal
42L AAPGAS[P/L]PSPGGDAAW 1
proximal
Showing 1 to 5 of 34 rows

PTM Site: 51S

Affected site:

Position: 51
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

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Mutation
In sequence
Distance
Impact
51G PGGDAAW[S/G]SEAGPGPR 0
direct
51I PGGDAAW[S/I]SEAGPGPR 0
direct
51R PGGDAAW[S/R]SEAGPGPR 0
direct
50R PGGDAA[W/R]WSEAGPGPR 1
proximal
50C PGGDAA[W/C]WSEAGPGPR 1
proximal
Showing 1 to 5 of 30 rows

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