Colon Cancer: Gene >> TSPAN8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247829
Start	71129335:71129335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774338946
CDS Mutation	c.656T>C
AA Mutation	p.Ile219Thr(p.I219T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247829
Start	71132816:71132816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000247829
Start	71129353:71129353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638C>A
AA Mutation	p.Ser213Ter(p.S213*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000247829
Start	71139710:71139710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000247829
Start	71157648:71157650(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.29_31delATT
AA Mutation	p.Tyr10del(p.Y10del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TSPAN8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247829
Start	71139790:71139790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.182C>T
AA Mutation	p.Ala61Val(p.A61V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript