Colon Cancer: Gene >> FOSL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264716
Start	28412063:28412063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143327177
CDS Mutation	c.596G>A
AA Mutation	p.Arg199Gln(p.R199Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264716
Start	28412118:28412118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142100731
CDS Mutation	c.651C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000264716
Start	28411930:28411930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463G>T
AA Mutation	p.Glu155Ter(p.E155*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000264716
Start	28411997:28411999(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.532_534delGAG
AA Mutation	p.Glu178del(p.E178del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FOSL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264716
Start	28404252:28404252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199613963
CDS Mutation	c.248G>T
AA Mutation	p.Ser83Ile(p.S83I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264716
Start	28404178:28404178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000264716
Start	28411963:28411983(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.509_529delTTGCTGAGCTGCAGAAGGAGA
AA Mutation	p.Ile170_Glu176del(p.I170_E176del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript