Colon Cancer: Gene >> SPRED3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338502
Start	38392102:38392102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760930195
CDS Mutation	c.334G>A
AA Mutation	p.Ala112Thr(p.A112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338502
Start	38395760:38395760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.848C>T
AA Mutation	p.Ala283Val(p.A283V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338502
Start	38394753:38394753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.534C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338502
Start	38390364:38390365(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.68dupG
AA Mutation	p.Gly24ArgfsTer63(p.G24Rfs*63)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SPRED3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338502
Start	38390419:38390419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757413877
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript