Colon Cancer: Gene >> RASL10B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000603017
Start	35741099:35741099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406C>T
AA Mutation	p.Arg136Cys(p.R136C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000603017
Start	35741102:35741102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781820562
CDS Mutation	c.409G>A
AA Mutation	p.Val137Met(p.V137M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000603017
Start	35735200:35735200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16C>T
AA Mutation	p.Arg6Trp(p.R6W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000603017
Start	35735389:35735389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205A>G
AA Mutation	p.Asn69Asp(p.N69D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000603017
Start	35735393:35735393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.209C>T
AA Mutation	p.Thr70Met(p.T70M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RASL10B

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000603017
Start	35741068:35741068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript