Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312693
Start	11269138:11269138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200495915
CDS Mutation	c.125G>A
AA Mutation	p.Arg42His(p.R42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312693
Start	11268887:11268887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376T>C
AA Mutation	p.Tyr126His(p.Y126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312693
Start	11269085:11269085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200118105
CDS Mutation	c.178A>G
AA Mutation	p.Thr60Ala(p.T60A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312693
Start	11269002:11269002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749116359
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312693
Start	11269179:11269179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TNP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312693
Start	11268874:11268874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367567297
CDS Mutation	c.389C>T
AA Mutation	p.Thr130Met(p.T130M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312693
Start	11269022:11269022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774953108
CDS Mutation	c.241C>T
AA Mutation	p.Arg81Cys(p.R81C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312693
Start	11269138:11269138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200495915
CDS Mutation	c.125G>A
AA Mutation	p.Arg42His(p.R42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript