Colon Cancer: Gene >> CNRIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263655
Start	68317183:68317183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139324099
CDS Mutation	c.304C>T
AA Mutation	p.Arg102Trp(p.R102W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263655
Start	68317218:68317218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269A>G
AA Mutation	p.Asp90Gly(p.D90G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263655
Start	68319310:68319310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748240304
CDS Mutation	c.91C>T
AA Mutation	p.Arg31Cys(p.R31C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263655
Start	68319305:68319305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754376239
CDS Mutation	c.96C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263655
Start	68317202:68317202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263655
Start	68319347:68319347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.54T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CNRIP1

No Mutation Annotation!