Colon Cancer: Gene >> CYP8B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316161
Start	42875401:42875401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.416T>G
AA Mutation	p.Leu139Arg(p.L139R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316161
Start	42874508:42874508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140045753
CDS Mutation	c.1309G>A
AA Mutation	p.Val437Ile(p.V437I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316161
Start	42875416:42875416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401A>G
AA Mutation	p.Asp134Gly(p.D134G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316161
Start	42875735:42875735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373922271
CDS Mutation	c.82C>T
AA Mutation	p.Arg28Cys(p.R28C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316161
Start	42875201:42875201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616T>A
AA Mutation	p.Phe206Ile(p.F206I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316161
Start	42874382:42874382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771278880
CDS Mutation	c.1435C>T
AA Mutation	p.Arg479Cys(p.R479C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000316161
Start	42874615:42874615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202C>T
AA Mutation	p.Thr401Ile(p.T401I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000316161
Start	42874411:42874411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1406A>G
AA Mutation	p.Asp469Gly(p.D469G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000316161
Start	42875740:42875740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779913482
CDS Mutation	c.77G>A
AA Mutation	p.Arg26Gln(p.R26Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316161
Start	42874461:42874461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1356C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316161
Start	42874497:42874497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1320C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316161
Start	42875259:42875259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150090141
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316161
Start	42875046:42875046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372142832
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316161
Start	42875502:42875502(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.315delA
AA Mutation	p.Lys105AsnfsTer4(p.K105Nfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000316161
Start	42875073:42875075(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs750438995
CDS Mutation	c.742_744delAAG
AA Mutation	p.Lys248del(p.K248del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CYP8B1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316161
Start	42874509:42874509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138292874
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript