Colon Cancer: Gene >> CDK5RAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338399
Start	47975581:47975581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581G>T
AA Mutation	p.Gly194Val(p.G194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338399
Start	47975199:47975199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375G>T
AA Mutation	p.Glu125Asp(p.E125D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338399
Start	47978889:47978889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778005374
CDS Mutation	c.1049G>A
AA Mutation	p.Arg350Gln(p.R350Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338399
Start	47976807:47976807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146603580
CDS Mutation	c.894G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338399
Start	47981493:47981493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1512C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CDK5RAP3

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000338399
Start	47975532:47975532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532G>T
AA Mutation	p.Glu178Ter(p.E178*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000338399
Start	47975966:47975966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751G>T
AA Mutation	p.Glu251Ter(p.E251*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript