Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CRKL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354336
Start	20933810:20933810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343G>A
AA Mutation	p.Ala115Thr(p.A115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354336
Start	20949778:20949778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845G>A
AA Mutation	p.Arg282His(p.R282H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354336
Start	20918070:20918070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136G>T
AA Mutation	p.Gly46Trp(p.G46W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354336
Start	20934081:20934081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614A>G
AA Mutation	p.His205Arg(p.H205R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354336
Start	20933901:20933901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434A>C
AA Mutation	p.Lys145Thr(p.K145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CRKL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354336
Start	20949765:20949765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832G>A
AA Mutation	p.Glu278Lys(p.E278K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354336
Start	20934169:20934169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354336
Start	20934187:20934187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755185083
CDS Mutation	c.720G>A
Mutation Classification	Silent
Feature Type	Transcript