Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FZD5

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295417
Start 207768498:207768498(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.242A>G
AA Mutation p.Asp81Gly(p.D81G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295417
Start 207767587:207767587(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1153C>A
AA Mutation p.Pro385Thr(p.P385T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295417
Start 207768393:207768393(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.347G>A
AA Mutation p.Cys116Tyr(p.C116Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000295417
Start 207767294:207767294(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1446C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000295417
Start 207767693:207767694(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1046dupG
AA Mutation p.Asn350GlnfsTer249(p.N350Qfs*249)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> FZD5

Mutation ID 1
Mutation Consequence synonymous_variant
Transcription ID ENST00000295417
Start 207767639:207767639(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1101C>T
Mutation Classification Silent
Feature Type Transcript