Colon Cancer: Gene >> SDF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360001
Start	1228526:1228526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268T>G
AA Mutation	p.Phe90Val(p.F90V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360001
Start	1217658:1217658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943G>A
AA Mutation	p.Ala315Thr(p.A315T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360001
Start	1218544:1218544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778380110
CDS Mutation	c.826G>A
AA Mutation	p.Asp276Asn(p.D276N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360001
Start	1217538:1217538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1063G>A
AA Mutation	p.Ala355Thr(p.A355T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360001
Start	1223302:1223302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360001
Start	1223284:1223284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145407954
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360001
Start	1218626:1218626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757831731
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SDF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360001
Start	1228624:1228624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170T>A
AA Mutation	p.Leu57Gln(p.L57Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript