Colon Cancer: Gene >> RHBDF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262316
Start	60460:60460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1637C>T
AA Mutation	p.Ser546Phe(p.S546F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262316
Start	61224:61224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1453G>A
AA Mutation	p.Val485Met(p.V485M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262316
Start	61453:61453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573506725
CDS Mutation	c.1327C>T
AA Mutation	p.Arg443Trp(p.R443W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262316
Start	64723:64723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224C>T
AA Mutation	p.Thr75Met(p.T75M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262316
Start	61244:61244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1433G>A
AA Mutation	p.Cys478Tyr(p.C478Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262316
Start	59451:59451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1861T>C
AA Mutation	p.Tyr621His(p.Y621H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262316
Start	63035:63035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140291610
CDS Mutation	c.610C>T
AA Mutation	p.Arg204Trp(p.R204W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262316
Start	58436:58436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2472C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262316
Start	58364:58364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2544C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262316
Start	58355:58355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144558704
CDS Mutation	c.2553C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262316
Start	61228:61228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1449G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RHBDF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262316
Start	59045:59045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2077G>A
AA Mutation	p.Ala693Thr(p.A693T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript