Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GIPC2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370759
Start 78135730:78135730(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765583476
CDS Mutation c.935G>A
AA Mutation p.Arg312Gln(p.R312Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000370759
Start 78119487:78119487(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.702C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000370759
Start 78095080:78095080(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.560delA
AA Mutation p.Lys187ArgfsTer7(p.K187Rfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 4
Mutation Consequence stop_gained
Transcription ID ENST00000370759
Start 78125947:78125947(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774818269
CDS Mutation c.781C>T
AA Mutation p.Arg261Ter(p.R261*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> GIPC2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370759
Start 78080777:78080777(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758543783
CDS Mutation c.343G>A
AA Mutation p.Glu115Lys(p.E115K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence stop_gained
Transcription ID ENST00000370759
Start 78119431:78119431(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140087680
CDS Mutation c.646G>T
AA Mutation p.Glu216Ter(p.E216*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript