Colon Cancer: Gene >> GOT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245206
Start	58716047:58716047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.986C>T
AA Mutation	p.Ala329Val(p.A329V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245206
Start	58716144:58716144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.889G>A
AA Mutation	p.Asp297Asn(p.D297N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000245206
Start	58722244:58722244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281A>G
AA Mutation	p.Lys94Arg(p.K94R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000245206
Start	58722252:58722252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273T>A
AA Mutation	p.Asn91Lys(p.N91K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000245206
Start	58716797:58716797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754471368
CDS Mutation	c.719C>T
AA Mutation	p.Ala240Val(p.A240V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245206
Start	58716796:58716796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758265732
CDS Mutation	c.720G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000245206
Start	58716012:58716012(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1019+2delT
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GOT2

No Mutation Annotation!