Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PDHA1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000422285
Start 19349340:19349340(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.86A>C
AA Mutation p.Asn29Thr(p.N29T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000422285
Start 19355484:19355484(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.739G>A
AA Mutation p.Asp247Asn(p.D247N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000422285
Start 19355482:19355482(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.737G>A
AA Mutation p.Gly246Asp(p.G246D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000422285
Start 19349357:19349357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.103A>G
AA Mutation p.Thr35Ala(p.T35A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000422285
Start 19355360:19355360(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs137853254
CDS Mutation c.615C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000422285
Start 19351358:19351358(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.369T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000422285
Start 19354565:19354565(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.585C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000422285
Start 19353111:19353111(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.448G>T
AA Mutation p.Gly150Ter(p.G150*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> PDHA1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000422285
Start 19350071:19350071(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.252G>T
AA Mutation p.Gln84His(p.Q84H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000422285
Start 19355438:19355438(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138237215
CDS Mutation c.693G>A
Mutation Classification Silent
Feature Type Transcript