Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DSTN

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000246069
Start 17604592:17604592(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.349T>C
AA Mutation p.Tyr117His(p.Y117H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000246069
Start 17601006:17601006(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.272C>T
AA Mutation p.Thr91Ile(p.T91I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000246069
Start 17601034:17601035(version: GRCh38)
Mutation Type INS
dbSNP_RS rs767965259
CDS Mutation c.308dupT
AA Mutation p.Leu103PhefsTer12(p.L103Ffs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> DSTN

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000246069
Start 17600795:17600795(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138670114
CDS Mutation c.61C>T
AA Mutation p.Arg21Cys(p.R21C)
Mutation Classification Missense_Mutation
Feature Type Transcript