Colon Cancer: Gene >> STRN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263918
Start	36893916:36893916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913G>T
AA Mutation	p.Gly305Cys(p.G305C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263918
Start	36925105:36925105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338G>T
AA Mutation	p.Arg113Ile(p.R113I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263918
Start	36869619:36869619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434G>T
AA Mutation	p.Leu478Phe(p.L478F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263918
Start	36899631:36899631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548893424
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263918
Start	36857926:36857926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1767A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263918
Start	36902661:36902661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747162112
CDS Mutation	c.582G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263918
Start	36886722:36886722(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1036delG
AA Mutation	p.Val346Ter(p.V346*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000263918
Start	36905556:36905556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.475C>T
AA Mutation	p.Arg159Ter(p.R159*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000263918
Start	36902583:36902583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> STRN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263918
Start	36857943:36857943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750T>G
AA Mutation	p.Leu584Val(p.L584V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263918
Start	36855255:36855255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1935A>C
AA Mutation	p.Glu645Asp(p.E645D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263918
Start	36883948:36883948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1170T>G
AA Mutation	p.Ile390Met(p.I390M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript