Colon Cancer: Gene >> NTN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293973
Start	2472797:2472797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141027585
CDS Mutation	c.1025G>A
AA Mutation	p.Arg342Gln(p.R342Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293973
Start	2472608:2472608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756784096
CDS Mutation	c.907C>T
AA Mutation	p.Arg303Trp(p.R303W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293973
Start	2472338:2472338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637G>T
AA Mutation	p.Asp213Tyr(p.D213Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000293973
Start	2472348:2472348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.647C>T
AA Mutation	p.Thr216Ile(p.T216I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293973
Start	2472559:2472559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293973
Start	2472182:2472182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293973
Start	2472433:2472433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293973
Start	2472058:2472058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774425636
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NTN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293973
Start	2472560:2472560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.859C>T
AA Mutation	p.Arg287Cys(p.R287C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript