Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CBLN4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000064571
Start	56000828:56000828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311A>T
AA Mutation	p.Asn104Ile(p.N104I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000064571
Start	56003901:56003901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Cys(p.R91C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000064571
Start	56003886:56003886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286G>A
AA Mutation	p.Asp96Asn(p.D96N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000064571
Start	55998577:55998577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586T>A
AA Mutation	p.Phe196Ile(p.F196I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000064571
Start	56003921:56003921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251C>G
AA Mutation	p.Ser84Cys(p.S84C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CBLN4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000064571
Start	55998711:55998711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452C>T
AA Mutation	p.Ala151Val(p.A151V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000064571
Start	56003958:56003958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756451061
CDS Mutation	c.214G>A
AA Mutation	p.Ala72Thr(p.A72T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000064571
Start	56003887:56003887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript