Colon Cancer: Gene >> NTN5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270235
Start	48663776:48663776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009G>T
AA Mutation	p.Gly337Cys(p.G337C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270235
Start	48670739:48670739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248G>A
AA Mutation	p.Cys83Tyr(p.C83Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270235
Start	48664741:48664741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.658C>T
AA Mutation	p.Arg220Cys(p.R220C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270235
Start	48670872:48670872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553526313
CDS Mutation	c.115G>A
AA Mutation	p.Val39Met(p.V39M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270235
Start	48670913:48670913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139966788
CDS Mutation	c.74G>A
AA Mutation	p.Arg25His(p.R25H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270235
Start	48670455:48670455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761654700
CDS Mutation	c.532C>T
AA Mutation	p.Arg178Cys(p.R178C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270235
Start	48670819:48670819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773395245
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270235
Start	48663780:48663780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005T>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NTN5

No Mutation Annotation!