Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FPR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339223
Start	51824461:51824461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764805147
CDS Mutation	c.713G>A
AA Mutation	p.Arg238His(p.R238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339223
Start	51824655:51824655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374026779
CDS Mutation	c.907G>A
AA Mutation	p.Val303Ile(p.V303I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339223
Start	51824044:51824044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296A>C
AA Mutation	p.Lys99Thr(p.K99T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339223
Start	51824139:51824139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391G>A
AA Mutation	p.Ala131Thr(p.A131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339223
Start	51824189:51824189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143644530
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339223
Start	51824420:51824420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339223
Start	51824622:51824622(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.879delT
AA Mutation	p.Phe293LeufsTer21(p.F293Lfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FPR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339223
Start	51824649:51824649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901C>A
AA Mutation	p.Leu301Ile(p.L301I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339223
Start	51824095:51824095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.347T>C
AA Mutation	p.Ile116Thr(p.I116T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339223
Start	51823990:51823990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757959263
CDS Mutation	c.242G>A
AA Mutation	p.Arg81Gln(p.R81Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript