Colon Cancer: Gene >> TAF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372977
Start	42077233:42077233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914G>T
AA Mutation	p.Arg305Met(p.R305M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372977
Start	42051417:42051417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106A>G
AA Mutation	p.Thr36Ala(p.T36A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372977
Start	42077107:42077107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788C>A
AA Mutation	p.Ser263Tyr(p.S263Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372977
Start	42051406:42051406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95C>T
AA Mutation	p.Ala32Val(p.A32V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372977
Start	42077118:42077118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799A>G
AA Mutation	p.Lys267Glu(p.K267E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TAF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372977
Start	42068583:42068583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756G>T
AA Mutation	p.Glu252Asp(p.E252D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372977
Start	42068514:42068514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565147111
CDS Mutation	c.687G>A
Mutation Classification	Silent
Feature Type	Transcript