Colon Cancer: Gene >> SELENBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368868
Start	151365636:151365636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971T>C
AA Mutation	p.Phe324Ser(p.F324S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368868
Start	151365582:151365582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1025G>T
AA Mutation	p.Arg342Ile(p.R342I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368868
Start	151364600:151364600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1362C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368868
Start	151365192:151365192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368868
Start	151365674:151365674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373594176
CDS Mutation	c.933C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SELENBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368868
Start	151366802:151366802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201828270
CDS Mutation	c.584G>A
AA Mutation	p.Arg195Gln(p.R195Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368868
Start	151364630:151364630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1332G>A
Mutation Classification	Silent
Feature Type	Transcript