Colon Cancer: Gene >> GSPT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000420576
Start	11885230:11885230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200641745
CDS Mutation	c.884A>G
AA Mutation	p.Asn295Ser(p.N295S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000420576
Start	11886583:11886583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727C>T
AA Mutation	p.Pro243Ser(p.P243S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000420576
Start	11887682:11887682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767004325
CDS Mutation	c.431G>A
AA Mutation	p.Arg144His(p.R144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420576
Start	11886923:11886923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GSPT1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420576
Start	11896637:11896637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.171C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420576
Start	11877575:11877575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377596394
CDS Mutation	c.1020C>T
Mutation Classification	Silent
Feature Type	Transcript