Colon Cancer: Gene >> CCRL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399036
Start	46408395:46408395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316C>A
AA Mutation	p.Leu106Ile(p.L106I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399036
Start	46408366:46408366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287A>G
AA Mutation	p.His96Arg(p.H96R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399036
Start	46408242:46408242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.163G>T
AA Mutation	p.Asp55Tyr(p.D55Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399036
Start	46409106:46409106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759009059
CDS Mutation	c.1027G>A
AA Mutation	p.Glu343Lys(p.E343K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399036
Start	46408465:46408465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.386A>G
AA Mutation	p.Tyr129Cys(p.Y129C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399036
Start	46408376:46408376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201907429
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCRL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399036
Start	46408699:46408699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200546954
CDS Mutation	c.620C>T
AA Mutation	p.Ser207Leu(p.S207L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript