Mutation

Primary Site >> Stomach Cancer

Gene >> NEIL2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284503
Start	11779710:11779710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251C>T
AA Mutation	p.Ala84Val(p.A84V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284503
Start	11786187:11786187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139505292
CDS Mutation	c.913G>A
AA Mutation	p.Glu305Lys(p.E305K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284503
Start	11779853:11779853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772930057
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Cys(p.R132C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284503
Start	11786152:11786152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878C>T
AA Mutation	p.Ala293Val(p.A293V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284503
Start	11786078:11786078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284503
Start	11779699:11779699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.240G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284503
Start	11779822:11779822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143923741
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284503
Start	11779741:11779741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284503
Start	11771523:11771523(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.80delG
AA Mutation	p.Gly27AlafsTer32(p.G27Afs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000284503
Start	11786133:11786133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859C>T
AA Mutation	p.Gln287Ter(p.Q287*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript