Colon Cancer: Gene >> FOSB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353609
Start	45471237:45471237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.491G>A
AA Mutation	p.Arg164Gln(p.R164Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000353609
Start	45471228:45471228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482G>A
AA Mutation	p.Arg161His(p.R161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000353609
Start	45472942:45472942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Gly316Asp(p.G316D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000353609
Start	45470794:45470794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763363699
CDS Mutation	c.292G>A
AA Mutation	p.Asp98Asn(p.D98N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000353609
Start	45472959:45472959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767173866
CDS Mutation	c.964G>A
AA Mutation	p.Gly322Ser(p.G322S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353609
Start	45472673:45472673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000353609
Start	45470773:45470773(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.275delC
AA Mutation	p.Pro92ArgfsTer18(p.P92Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FOSB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353609
Start	45472634:45472634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.639T>G
AA Mutation	p.Phe213Leu(p.F213L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript