Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CRLF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381566
Start	1202502:1202502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383C>T
AA Mutation	p.Ser128Leu(p.S128L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381566
Start	1198565:1198565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759127718
CDS Mutation	c.643C>T
AA Mutation	p.Arg215Trp(p.R215W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381566
Start	1202501:1202501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778697451
CDS Mutation	c.384G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381566
Start	1206452:1206452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CRLF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381566
Start	1198565:1198565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759127718
CDS Mutation	c.643C>T
AA Mutation	p.Arg215Trp(p.R215W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381566
Start	1208829:1208829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.159G>A
Mutation Classification	Silent
Feature Type	Transcript