Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PINX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314787
Start	10765454:10765454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372632631
CDS Mutation	c.934G>A
AA Mutation	p.Ala312Thr(p.A312T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314787
Start	10765837:10765837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551A>C
AA Mutation	p.Lys184Thr(p.K184T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314787
Start	10765438:10765438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779941568
CDS Mutation	c.950C>T
AA Mutation	p.Thr317Met(p.T317M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314787
Start	10765677:10765677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.711G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314787
Start	10765623:10765623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780628077
CDS Mutation	c.765G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PINX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314787
Start	10765454:10765454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372632631
CDS Mutation	c.934G>A
AA Mutation	p.Ala312Thr(p.A312T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314787
Start	10765875:10765875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374083715
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript