Colon Cancer: Gene >> FFAR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246549
Start	35450099:35450099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385G>A
AA Mutation	p.Ala129Thr(p.A129T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246549
Start	35450057:35450057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774217360
CDS Mutation	c.343G>A
AA Mutation	p.Val115Met(p.V115M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246549
Start	35450616:35450616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147802928
CDS Mutation	c.902G>A
AA Mutation	p.Arg301His(p.R301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246549
Start	35450363:35450363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200165905
CDS Mutation	c.649C>T
AA Mutation	p.Arg217Trp(p.R217W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246549
Start	35450419:35450419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246549
Start	35449927:35449927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373797261
CDS Mutation	c.213G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246549
Start	35450437:35450437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246549
Start	35449812:35449813(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.102dupG
AA Mutation	p.Arg35AlafsTer120(p.R35Afs*120)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FFAR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246549
Start	35450153:35450153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771781550
CDS Mutation	c.439G>A
AA Mutation	p.Val147Ile(p.V147I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246549
Start	35449923:35449923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775045094
CDS Mutation	c.209C>T
AA Mutation	p.Ala70Val(p.A70V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246549
Start	35450236:35450236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546200557
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246549
Start	35449927:35449927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373797261
CDS Mutation	c.213G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246549
Start	35450080:35450080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246549
Start	35450623:35450623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.909C>G
Mutation Classification	Silent
Feature Type	Transcript