Colon Cancer: Gene >> OXTR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316793
Start	8753020:8753020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769146293
CDS Mutation	c.1127G>A
AA Mutation	p.Arg376His(p.R376H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316793
Start	8767533:8767533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655T>G
AA Mutation	p.Cys219Gly(p.C219G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316793
Start	8753132:8753132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143927655
CDS Mutation	c.1015G>A
AA Mutation	p.Glu339Lys(p.E339K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316793
Start	8753013:8753013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746072418
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316793
Start	8767870:8767870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OXTR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316793
Start	8767374:8767374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Cys(p.R272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript