Mutation

Primary Site >> Stomach Cancer

Gene >> SEC23IP

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119929625:119929625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2332T>G
AA Mutation	p.Ser778Ala(p.S778A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119898546:119898546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283A>G
AA Mutation	p.Asn95Asp(p.N95D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119914790:119914790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1373A>G
AA Mutation	p.Asp458Gly(p.D458G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119904129:119904129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.953G>A
AA Mutation	p.Arg318His(p.R318H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119918407:119918407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1768T>A
AA Mutation	p.Phe590Ile(p.F590I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119917985:119917985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1694T>A
AA Mutation	p.Leu565His(p.L565H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369075
Start	119898814:119898814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551G>A
AA Mutation	p.Arg184His(p.R184H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369075
Start	119892815:119892815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761614545
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369075
Start	119898641:119898641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369075
Start	119898608:119898608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369075
Start	119898533:119898533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000369075
Start	119932174:119932174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2614C>T
AA Mutation	p.Gln872Ter(p.Q872*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000369075
Start	119904279:119904279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1101+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript