Colon Cancer: Gene >> GPBAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000479077
Start	218263259:218263259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535G>T
AA Mutation	p.Gly179Cys(p.G179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000479077
Start	218263229:218263229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200096596
CDS Mutation	c.505G>A
AA Mutation	p.Glu169Lys(p.E169K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000479077
Start	218262729:218262729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5C>T
AA Mutation	p.Thr2Met(p.T2M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479077
Start	218263498:218263498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479077
Start	218263252:218263252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202154681
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPBAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000479077
Start	218263488:218263488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769777368
CDS Mutation	c.764C>T
AA Mutation	p.Pro255Leu(p.P255L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000479077
Start	218262731:218262731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7C>T
AA Mutation	p.Pro3Ser(p.P3S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000479077
Start	218263516:218263516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript