Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> WNT9B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290015
Start	46875325:46875325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200104547
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Trp(p.R187W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290015
Start	46875227:46875227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756222047
CDS Mutation	c.461G>C
AA Mutation	p.Arg154Pro(p.R154P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290015
Start	46875175:46875175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202125492
CDS Mutation	c.409G>A
AA Mutation	p.Ala137Thr(p.A137T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290015
Start	46872685:46872685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373305196
CDS Mutation	c.246G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290015
Start	46875216:46875216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.450G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290015
Start	46875141:46875141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368158766
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000290015
Start	46875168:46875169(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.402_403insAGGGTG
AA Mutation	p.Ala134_Cys135insArgVal(p.A134_C135insRV)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> WNT9B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290015
Start	46875325:46875325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200104547
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Trp(p.R187W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290015
Start	46876615:46876615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971G>A
AA Mutation	p.Ser324Asn(p.S324N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290015
Start	46872532:46872532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.93A>C
AA Mutation	p.Glu31Asp(p.E31D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript