Mutation

Primary Site >> Stomach Cancer

Gene >> CNDP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74562073:74562073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146707393
CDS Mutation	c.493G>A
AA Mutation	p.Asp165Asn(p.D165N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74560884:74560884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332C>A
AA Mutation	p.Pro111His(p.P111H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74567276:74567276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.599A>G
AA Mutation	p.Glu200Gly(p.E200G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74567408:74567408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750904832
CDS Mutation	c.731G>A
AA Mutation	p.Arg244Gln(p.R244Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74562097:74562097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758303238
CDS Mutation	c.517T>C
AA Mutation	p.Trp173Arg(p.W173R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74560970:74560970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371268412
CDS Mutation	c.418C>T
AA Mutation	p.Arg140Trp(p.R140W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358821
Start	74556346:74556346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358821
Start	74534686:74534686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000358821
Start	74560958:74560958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406C>T
AA Mutation	p.Gln136Ter(p.Q136*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript