Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RAB5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273047
Start	19976070:19976070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339T>A
AA Mutation	p.Asn113Lys(p.N113K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273047
Start	19976135:19976135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404C>T
AA Mutation	p.Ala135Val(p.A135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273047
Start	19976143:19976143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760110691
CDS Mutation	c.412G>A
AA Mutation	p.Ala138Thr(p.A138T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273047
Start	19976149:19976149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418A>G
AA Mutation	p.Lys140Glu(p.K140E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273047
Start	19976067:19976067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RAB5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273047
Start	19975705:19975705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268T>A
AA Mutation	p.Tyr90Asn(p.Y90N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273047
Start	19976070:19976070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339T>A
AA Mutation	p.Asn113Lys(p.N113K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript