Colon Cancer: Gene >> SOX15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250055
Start	7589247:7589247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430G>A
AA Mutation	p.Gly144Ser(p.G144S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250055
Start	7589578:7589578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99G>T
AA Mutation	p.Glu33Asp(p.E33D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250055
Start	7589349:7589349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250055
Start	7589638:7589638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250055
Start	7589179:7589179(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.498delC
AA Mutation	p.Ser167AlafsTer64(p.S167Afs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250055
Start	7588442:7588442(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.638delC
AA Mutation	p.Pro213LeufsTer18(p.P213Lfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SOX15

Mutation ID	1
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000250055
Start	7589533:7589535(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.142_144delAAG
AA Mutation	p.Lys48del(p.K48del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript