Colon Cancer: Gene >> GFI1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339463
Start	132991001:132991001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761729738
CDS Mutation	c.944G>A
AA Mutation	p.Arg315His(p.R315H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339463
Start	132991018:132991018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765068455
CDS Mutation	c.961C>T
AA Mutation	p.Arg321Trp(p.R321W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339463
Start	132987412:132987412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768614274
CDS Mutation	c.231G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GFI1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339463
Start	132989142:132989142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370269669
CDS Mutation	c.592G>A
AA Mutation	p.Gly198Ser(p.G198S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339463
Start	132989066:132989066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516C>A
AA Mutation	p.Phe172Leu(p.F172L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339463
Start	132991035:132991035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.978G>T
AA Mutation	p.Gln326His(p.Q326H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript