Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HDGF

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000357325
Start 156745297:156745297(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.164C>T
AA Mutation p.Thr55Met(p.T55M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357325
Start 156744266:156744266(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.386C>T
AA Mutation p.Ala129Val(p.A129V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357325
Start 156743847:156743847(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.521A>C
AA Mutation p.Asn174Thr(p.N174T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000357325
Start 156745308:156745308(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.153G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000357325
Start 156745312:156745312(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.149delT
AA Mutation p.Phe50SerfsTer105(p.F50Sfs*105)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000357325
Start 156745311:156745312(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.149dupT
AA Mutation p.Gly51ArgfsTer63(p.G51Rfs*63)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> HDGF

No Mutation Annotation!