Colon Cancer: Gene >> SLC10A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216540
Start	69776347:69776347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985A>G
AA Mutation	p.Thr329Ala(p.T329A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216540
Start	69797094:69797094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200122790
CDS Mutation	c.62G>A
AA Mutation	p.Arg21His(p.R21H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216540
Start	69797150:69797150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6G>T
AA Mutation	p.Glu2Asp(p.E2D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216540
Start	69797072:69797072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216540
Start	69776306:69776306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1026G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC10A1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000216540
Start	69779183:69779183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76966244
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Trp(p.R249W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216540
Start	69797133:69797133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201015997
CDS Mutation	c.23C>T
AA Mutation	p.Ala8Val(p.A8V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216540
Start	69786229:69786229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>A
Mutation Classification	Silent
Feature Type	Transcript