Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FCER2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346664
Start	7689371:7689371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777512868
CDS Mutation	c.788G>A
AA Mutation	p.Arg263Gln(p.R263Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346664
Start	7689309:7689309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780858530
CDS Mutation	c.850C>T
AA Mutation	p.Arg284Trp(p.R284W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346664
Start	7698781:7698781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185214885
CDS Mutation	c.96C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346664
Start	7690203:7690203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000346664
Start	7697590:7697590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FCER2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346664
Start	7699748:7699748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13C>A
AA Mutation	p.Gln5Lys(p.Q5K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346664
Start	7690513:7690513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145289159
CDS Mutation	c.514C>T
AA Mutation	p.Arg172Trp(p.R172W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346664
Start	7689216:7689216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943C>T
AA Mutation	p.Pro315Ser(p.P315S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346664
Start	7689274:7689274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885T>C
Mutation Classification	Silent
Feature Type	Transcript