Colon Cancer: Gene >> PTBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349038
Start	805112:805112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817C>A
AA Mutation	p.Arg273Ser(p.R273S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000349038
Start	808413:808413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129G>A
AA Mutation	p.Ala377Thr(p.A377T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000349038
Start	804119:804119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199C>T
AA Mutation	p.Pro67Ser(p.P67S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000349038
Start	805080:805080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785G>A
AA Mutation	p.Ser262Asn(p.S262N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349038
Start	806463:806463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349038
Start	810594:810594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372458011
CDS Mutation	c.1437C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349038
Start	805177:805177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752233494
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349038
Start	804930:804930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762173288
CDS Mutation	c.708C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349038
Start	808667:808667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376590892
CDS Mutation	c.1290C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTBP1

No Mutation Annotation!