Colon Cancer: Gene >> SAC3D1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000614106
Start	65044542:65044542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775031585
CDS Mutation	c.1030G>A
AA Mutation	p.Gly344Arg(p.G344R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000614106
Start	65044656:65044656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374748039
CDS Mutation	c.1144C>T
AA Mutation	p.Arg382Cys(p.R382C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000614106
Start	65044332:65044332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820G>A
AA Mutation	p.Ala274Thr(p.A274T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614106
Start	65044514:65044514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1002G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614106
Start	65044556:65044556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375977369
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614106
Start	65044583:65044583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1071G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000614106
Start	65044622:65044622(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1110delG
AA Mutation	p.Cys371AlafsTer4(p.C371Afs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SAC3D1

No Mutation Annotation!