Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FECH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262093
Start	57554913:57554913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770820411
CDS Mutation	c.844G>A
AA Mutation	p.Ala282Thr(p.A282T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262093
Start	57562936:57562936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746310270
CDS Mutation	c.643C>T
AA Mutation	p.Arg215Trp(p.R215W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262093
Start	57554937:57554937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146269992
CDS Mutation	c.820G>A
AA Mutation	p.Asp274Asn(p.D274N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262093
Start	57580174:57580174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.93T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262093
Start	57550766:57550766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1218T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262093
Start	57554359:57554359(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.978delG
AA Mutation	p.Arg327GlyfsTer9(p.R327Gfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FECH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262093
Start	57571456:57571456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.399G>T
AA Mutation	p.Lys133Asn(p.K133N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262093
Start	57554305:57554305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140758357
CDS Mutation	c.1032G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262093
Start	57554389:57554389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375689425
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript