Colon Cancer: Gene >> SCGN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377961
Start	25689188:25689188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>A
AA Mutation	p.Glu182Lys(p.E182K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377961
Start	25664994:25664994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567158105
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Trp(p.R100W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377961
Start	25664957:25664957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261C>A
AA Mutation	p.Phe87Leu(p.F87L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377961
Start	25664991:25664991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200726171
CDS Mutation	c.295C>T
AA Mutation	p.Arg99Cys(p.R99C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377961
Start	25653411:25653411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112G>A
AA Mutation	p.Asp38Asn(p.D38N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377961
Start	25669518:25669518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344G>A
AA Mutation	p.Arg115His(p.R115H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377961
Start	25701245:25701245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.741G>T
AA Mutation	p.Glu247Asp(p.E247D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377961
Start	25691094:25691094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000377961
Start	25670008:25670008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756848200
CDS Mutation	c.403C>T
AA Mutation	p.Arg135Ter(p.R135*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SCGN

No Mutation Annotation!