Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TTPAL

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262605
Start 44480262:44480262(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768842525
CDS Mutation c.263G>A
AA Mutation p.Arg88His(p.R88H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262605
Start 44480276:44480276(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.277G>A
AA Mutation p.Asp93Asn(p.D93N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262605
Start 44480196:44480196(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.197G>A
AA Mutation p.Arg66Gln(p.R66Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262605
Start 44480264:44480264(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.265A>G
AA Mutation p.Lys89Glu(p.K89E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000262605
Start 44480218:44480218(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.219C>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> TTPAL

No Mutation Annotation!