Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BTNL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374993
Start	32403044:32403044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600C>A
AA Mutation	p.Phe200Leu(p.F200L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374993
Start	32403084:32403084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.560C>T
AA Mutation	p.Ala187Val(p.A187V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374993
Start	32402975:32402975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374993
Start	32405150:32405150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BTNL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374993
Start	32396299:32396299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138515121
CDS Mutation	c.818C>T
AA Mutation	p.Ala273Val(p.A273V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374993
Start	32396078:32396078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039G>T
AA Mutation	p.Asp347Tyr(p.D347Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374993
Start	32396383:32396383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.734C>A
AA Mutation	p.Ser245Tyr(p.S245Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374993
Start	32403204:32403204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.440C>A
AA Mutation	p.Ala147Asp(p.A147D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript