Colon Cancer: Gene >> OR1B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304833
Start	122628922:122628922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.614T>C
AA Mutation	p.Ile205Thr(p.I205T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304833
Start	122629054:122629054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377379891
CDS Mutation	c.482G>A
AA Mutation	p.Arg161His(p.R161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304833
Start	122628811:122628811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759389860
CDS Mutation	c.725G>A
AA Mutation	p.Arg242Gln(p.R242Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304833
Start	122628790:122628790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746C>T
AA Mutation	p.Ser249Phe(p.S249F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304833
Start	122628916:122628916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.620T>C
AA Mutation	p.Phe207Ser(p.F207S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304833
Start	122628783:122628783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304833
Start	122628699:122628699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304833
Start	122628595:122628595(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.941delT
AA Mutation	p.Val314GlyfsTer3(p.V314Gfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> OR1B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304833
Start	122629112:122629112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139868007
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Trp(p.R142W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304833
Start	122629522:122629522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14C>T
AA Mutation	p.Ala5Val(p.A5V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304833
Start	122629243:122629243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754990888
CDS Mutation	c.293G>A
AA Mutation	p.Arg98His(p.R98H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304833
Start	122628815:122628815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140862378
CDS Mutation	c.721C>T
AA Mutation	p.Arg241Cys(p.R241C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript