Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ALDH3A1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000225740
Start 19742585:19742585(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs545815877
CDS Mutation c.440C>T
AA Mutation p.Ala147Val(p.A147V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000225740
Start 19742124:19742124(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780443108
CDS Mutation c.569C>T
AA Mutation p.Thr190Met(p.T190M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000225740
Start 19740344:19740344(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.941G>A
AA Mutation p.Arg314His(p.R314H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000225740
Start 19743286:19743286(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.340T>C
AA Mutation p.Trp114Arg(p.W114R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000225740
Start 19740419:19740419(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs115638369
CDS Mutation c.866G>A
AA Mutation p.Arg289Gln(p.R289Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000225740
Start 19742038:19742038(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774092621
CDS Mutation c.655G>A
AA Mutation p.Val219Met(p.V219M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000225740
Start 19742150:19742150(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202069113
CDS Mutation c.543C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000225740
Start 19743416:19743416(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.210G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000225740
Start 19738336:19738336(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs778623472
CDS Mutation c.1334delC
AA Mutation p.Pro445ArgfsTer6(p.P445Rfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000225740
Start 19739527:19739527(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1097delT
AA Mutation p.Met366SerfsTer8(p.M366Sfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000225740
Start 19743460:19743460(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778654435
CDS Mutation c.166G>T
AA Mutation p.Glu56Ter(p.E56*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> ALDH3A1

No Mutation Annotation!