Colon Cancer: Gene >> EFNB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245323
Start	106493147:106493147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770833245
CDS Mutation	c.895G>A
AA Mutation	p.Val299Ile(p.V299I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245323
Start	106493208:106493208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748940240
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245323
Start	106493196:106493196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113878095
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245323
Start	106512794:106512794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EFNB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245323
Start	106494913:106494913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581C>T
AA Mutation	p.Ser194Leu(p.S194L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245323
Start	106494908:106494908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.586A>G
AA Mutation	p.Thr196Ala(p.T196A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245323
Start	106495806:106495806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript