Colon Cancer: Gene >> GLRA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218075
Start	14530091:14530091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34T>A
AA Mutation	p.Leu12Met(p.L12M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218075
Start	14574378:14574378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248G>T
AA Mutation	p.Gly83Val(p.G83V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000218075
Start	14609129:14609129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854C>A
AA Mutation	p.Ala285Asp(p.A285D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000218075
Start	14730441:14730441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315A>T
AA Mutation	p.Ile439Phe(p.I439F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000218075
Start	14730223:14730223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1097G>A
AA Mutation	p.Arg366His(p.R366H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218075
Start	14532294:14532294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751025273
CDS Mutation	c.124C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218075
Start	14730473:14730473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1347C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000218075
Start	14607184:14607184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631C>T
AA Mutation	p.Gln211Ter(p.Q211*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GLRA2

No Mutation Annotation!