Colon Cancer: Gene >> ESRRA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000000442
Start	64315037:64315037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.779T>C
AA Mutation	p.Val260Ala(p.V260A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000000442
Start	64315160:64315160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902G>A
AA Mutation	p.Gly301Asp(p.G301D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000000442
Start	64315033:64315033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775T>C
AA Mutation	p.Ser259Pro(p.S259P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000000442
Start	64315047:64315047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.789C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000000442
Start	64315862:64315862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1168C>T
AA Mutation	p.Gln390Ter(p.Q390*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ESRRA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000000442
Start	64315084:64315084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767507136
CDS Mutation	c.826C>T
AA Mutation	p.Arg276Cys(p.R276C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000000442
Start	64307195:64307195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16G>A
AA Mutation	p.Val6Met(p.V6M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript