Colon Cancer: Gene >> SEPT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350320
Start	35883967:35883967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800A>G
AA Mutation	p.Tyr267Cys(p.Y267C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350320
Start	35903086:35903086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382His(p.R382H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350320
Start	35832823:35832823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92T>G
AA Mutation	p.Val31Gly(p.V31G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350320
Start	35903085:35903085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761757988
CDS Mutation	c.1144C>T
AA Mutation	p.Arg382Cys(p.R382C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350320
Start	35903147:35903147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350320
Start	35832887:35832887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779175492
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000350320
Start	35882577:35882577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SEPT7

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000350320
Start	35903127:35903127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1186G>T
AA Mutation	p.Glu396Ter(p.E396*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript