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Mutation:
MLH1 H473Y
Summary
Isoform:
Position:
473
Ref:
H
Mutation:
Y
PTM impact:
distal
PTM affected:
1
Kinases:
CSNK2A1
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
Hereditary nonpolyposis colorectal neoplasms, Hereditary cancer-predisposing syndrome
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 477S
Affected site:
Position: 477
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
471E | R[K/E]KRHREDSDVEMVED | 6 |
distal
|
472K | RK[R/K]RHREDSDVEMVED | 5 |
distal
|
473Y | RKR[H/Y]HREDSDVEMVED | 4 |
distal
|
473R | RKR[H/R]HREDSDVEMVED | 4 |
distal
|
474G | RKRH[R/G]REDSDVEMVED | 3 |
network-rewiring
|
474W | RKRH[R/W]REDSDVEMVED | 3 |
network-rewiring
|
474Q | RKRH[R/Q]REDSDVEMVED | 3 |
network-rewiring
|
478Y | RKRHREDS[D/Y]DVEMVED | 1 |
proximal
|
478V | RKRHREDS[D/V]DVEMVED | 1 |
proximal
|
479L | RKRHREDSD[V/L]VEMVED | 2 |
proximal
|
481V | RKRHREDSDVE[M/V]MVED | 4 |
distal
|
481T | RKRHREDSDVE[M/T]MVED | 4 |
distal
|
481I | RKRHREDSDVE[M/I]MVED | 4 |
distal
|
482M | RKRHREDSDVEM[V/M]VED | 5 |
distal
|
482L | RKRHREDSDVEM[V/L]VED | 5 |
distal
|
482A | RKRHREDSDVEM[V/A]VED | 5 |
distal
|
483K | RKRHREDSDVEMV[E/K]ED | 6 |
distal
|
External references
dbSNP:
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