Colon Cancer: Gene >> FPR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746573:51746573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422T>A
AA Mutation	p.Leu141Gln(p.L141Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746616:51746616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186613919
CDS Mutation	c.379G>A
AA Mutation	p.Val127Ile(p.V127I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746289:51746289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706T>A
AA Mutation	p.Ser236Thr(p.S236T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746585:51746585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745998725
CDS Mutation	c.410G>A
AA Mutation	p.Arg137His(p.R137H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746282:51746282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368075541
CDS Mutation	c.713G>A
AA Mutation	p.Arg238His(p.R238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746793:51746793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202G>A
AA Mutation	p.Ala68Thr(p.A68T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304748
Start	51746362:51746362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750529946
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304748
Start	51746257:51746257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148898220
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FPR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746715:51746715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>A
AA Mutation	p.Gly94Ser(p.G94S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746646:51746646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547228145
CDS Mutation	c.349G>A
AA Mutation	p.Ala117Thr(p.A117T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746052:51746052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140083445
CDS Mutation	c.943G>A
AA Mutation	p.Ala315Thr(p.A315T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript