Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CYP2W1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308919
Start	985222:985222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544C>T
AA Mutation	p.Leu182Phe(p.L182F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308919
Start	983216:983216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5C>A
AA Mutation	p.Ala2Asp(p.A2D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308919
Start	984431:984431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.194C>T
AA Mutation	p.Pro65Leu(p.P65L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308919
Start	986654:986654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676C>A
AA Mutation	p.Leu226Met(p.L226M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308919
Start	985215:985215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769443714
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308919
Start	983305:983305(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs745432053
CDS Mutation	c.98delC
AA Mutation	p.Pro33ArgfsTer24(p.P33Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CYP2W1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308919
Start	985310:985310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632C>T
AA Mutation	p.Ser211Phe(p.S211F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308919
Start	984421:984421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.184C>T
AA Mutation	p.Arg62Cys(p.R62C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308919
Start	985238:985238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560G>A
AA Mutation	p.Arg187Gln(p.R187Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript