Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> OSER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255174
Start	44197516:44197516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777251819
CDS Mutation	c.415G>A
AA Mutation	p.Asp139Asn(p.D139N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255174
Start	44203007:44203007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.145G>T
AA Mutation	p.Asp49Tyr(p.D49Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255174
Start	44206949:44206949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774147753
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255174
Start	44197571:44197571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.360G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255174
Start	44197634:44197634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748114723
CDS Mutation	c.297G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OSER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255174
Start	44197705:44197705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.226A>G
AA Mutation	p.Thr76Ala(p.T76A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255174
Start	44197298:44197298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633T>A
AA Mutation	p.Asp211Glu(p.D211E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255174
Start	44197158:44197158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773G>A
AA Mutation	p.Arg258Gln(p.R258Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript