Colon Cancer: Gene >> BATF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301887
Start	64989311:64989311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643A>G
AA Mutation	p.Thr215Ala(p.T215A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301887
Start	64989337:64989337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617C>T
AA Mutation	p.Pro206Leu(p.P206L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301887
Start	64989253:64989253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377505280
CDS Mutation	c.701G>A
AA Mutation	p.Arg234His(p.R234H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301887
Start	64989721:64989721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233A>G
AA Mutation	p.His78Arg(p.H78R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301887
Start	64989417:64989417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768550449
CDS Mutation	c.537G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301887
Start	64989372:64989372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301887
Start	64989549:64989549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BATF2

No Mutation Annotation!