Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HTR1D

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374619
Start 23193775:23193775(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761191232
CDS Mutation c.445C>T
AA Mutation p.Arg149Cys(p.R149C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374619
Start 23193931:23193931(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs41268111
CDS Mutation c.289G>A
AA Mutation p.Ala97Thr(p.A97T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000374619
Start 23193420:23193420(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376034704
CDS Mutation c.800C>T
AA Mutation p.Ser267Leu(p.S267L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000374619
Start 23193756:23193756(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780794417
CDS Mutation c.464C>T
AA Mutation p.Ala155Val(p.A155V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000374619
Start 23193293:23193293(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.927C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000374619
Start 23193702:23193702(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.518delC
AA Mutation p.Pro173ArgfsTer18(p.P173Rfs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> HTR1D

No Mutation Annotation!