Colon Cancer: Gene >> RAI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331511
Start	17800678:17800678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1333G>T
AA Mutation	p.Asp445Tyr(p.D445Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331511
Start	17801788:17801788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.223G>A
AA Mutation	p.Ala75Thr(p.A75T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331511
Start	17801790:17801790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771404978
CDS Mutation	c.221C>T
AA Mutation	p.Ala74Val(p.A74V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331511
Start	17800711:17800711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1300T>A
AA Mutation	p.Ser434Thr(p.S434T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331511
Start	17800591:17800591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147416008
CDS Mutation	c.1420G>A
AA Mutation	p.Val474Met(p.V474M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331511
Start	17800857:17800857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154C>A
AA Mutation	p.Ser385Tyr(p.S385Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331511
Start	17801094:17801094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146607759
CDS Mutation	c.917C>T
AA Mutation	p.Thr306Met(p.T306M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331511
Start	17801480:17801480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199687946
CDS Mutation	c.531G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331511
Start	17800592:17800592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1419C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331511
Start	17801216:17801216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.795C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RAI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331511
Start	17800828:17800828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1183C>A
AA Mutation	p.Pro395Thr(p.P395T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331511
Start	17800959:17800959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140631545
CDS Mutation	c.1052G>A
AA Mutation	p.Arg351Gln(p.R351Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331511
Start	17800640:17800640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1371C>G
Mutation Classification	Silent
Feature Type	Transcript