Colon Cancer: Gene >> CCR10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332438
Start	42680343:42680343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299C>T
AA Mutation	p.Ala100Val(p.A100V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332438
Start	42680428:42680428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>A
AA Mutation	p.Ala72Thr(p.A72T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332438
Start	42680381:42680381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332438
Start	42679603:42679603(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1039delT
AA Mutation	p.Ser347LeufsTer27(p.S347Lfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CCR10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332438
Start	42679717:42679717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925C>A
AA Mutation	p.Leu309Ile(p.L309I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript