Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KRT14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000167586
Start	41582499:41582499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1355T>C
AA Mutation	p.Val452Ala(p.V452A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000167586
Start	41586617:41586617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218T>A
AA Mutation	p.Phe73Tyr(p.F73Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000167586
Start	41586763:41586763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000167586
Start	41586523:41586523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371274993
CDS Mutation	c.312T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000167586
Start	41586635:41586635(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769596857
CDS Mutation	c.200delG
AA Mutation	p.Gly67AlafsTer51(p.G67Afs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KRT14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000167586
Start	41586354:41586354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481G>T
AA Mutation	p.Asp161Tyr(p.D161Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000167586
Start	41586361:41586361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474G>T
AA Mutation	p.Glu158Asp(p.E158D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000167586
Start	41586465:41586465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757852003
CDS Mutation	c.370G>A
AA Mutation	p.Asp124Asn(p.D124N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000167586
Start	41582461:41582461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1393G>A
AA Mutation	p.Glu465Lys(p.E465K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000167586
Start	41583769:41583769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918C>A
AA Mutation	p.Phe306Leu(p.F306L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript