Colon Cancer: Gene >> FPR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340023
Start	51769565:51769565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373596683
CDS Mutation	c.907G>A
AA Mutation	p.Val303Ile(p.V303I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340023
Start	51768945:51768945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287T>C
AA Mutation	p.Phe96Ser(p.F96S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340023
Start	51768828:51768828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750225501
CDS Mutation	c.170G>A
AA Mutation	p.Arg57His(p.R57H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340023
Start	51769371:51769371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199892175
CDS Mutation	c.713G>A
AA Mutation	p.Arg238His(p.R238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340023
Start	51769401:51769401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.743C>T
AA Mutation	p.Ala248Val(p.A248V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340023
Start	51769194:51769194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536A>T
AA Mutation	p.Asn179Ile(p.N179I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340023
Start	51769663:51769663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140469815
CDS Mutation	c.1005G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340023
Start	51769339:51769339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754054611
CDS Mutation	c.681G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340023
Start	51769485:51769486(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.827_828insCAATG
AA Mutation	p.Lys276AsnfsTer40(p.K276Nfs*40)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FPR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340023
Start	51769172:51769172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514G>T
AA Mutation	p.Gly172Trp(p.G172W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340023
Start	51769371:51769371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199892175
CDS Mutation	c.713G>A
AA Mutation	p.Arg238His(p.R238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000340023
Start	51768710:51768710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.52G>T
AA Mutation	p.Glu18Ter(p.E18*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript