Colon Cancer: Gene >> RPRM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325926
Start	153478402:153478402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753673954
CDS Mutation	c.164G>A
AA Mutation	p.Arg55His(p.R55H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325926
Start	153478550:153478550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16G>A
AA Mutation	p.Gly6Ser(p.G6S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325926
Start	153478440:153478440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.126G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325926
Start	153478338:153478338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200090187
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325926
Start	153478341:153478341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758425987
CDS Mutation	c.225C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RPRM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325926
Start	153478276:153478276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201295005
CDS Mutation	c.290C>T
AA Mutation	p.Pro97Leu(p.P97L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript