Mutation

Primary Site >> Stomach Cancer

Gene >> CELF2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11275102:11275102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573495632
CDS Mutation	c.802G>A
AA Mutation	p.Gly268Ser(p.G268S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11165622:11165622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190G>A
AA Mutation	p.Gly64Arg(p.G64R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11321354:11321354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1223A>C
AA Mutation	p.Gln408Pro(p.Q408P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11217436:11217436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577233700
CDS Mutation	c.262G>A
AA Mutation	p.Val88Ile(p.V88I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11321375:11321375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1244G>T
AA Mutation	p.Ser415Ile(p.S415I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11270702:11270702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634A>G
AA Mutation	p.Thr212Ala(p.T212A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416382
Start	11314252:11314252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416382
Start	11321322:11321322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374713225
CDS Mutation	c.1191G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416382
Start	11321244:11321244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1113C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000416382
Start	11325915:11325915(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1338delT
AA Mutation	p.Phe446LeufsTer17(p.F446Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000416382
Start	11288416:11288416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript