Mutation

Primary Site >> Stomach Cancer

Gene >> STAM

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377524
Start	17714587:17714587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370940096
CDS Mutation	c.1430C>T
AA Mutation	p.Ala477Val(p.A477V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377524
Start	17700262:17700262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895C>T
AA Mutation	p.Pro299Ser(p.P299S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377524
Start	17695156:17695156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643G>A
AA Mutation	p.Val215Ile(p.V215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377524
Start	17700266:17700266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899C>T
AA Mutation	p.Ala300Val(p.A300V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377524
Start	17704449:17704449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931C>A
AA Mutation	p.Leu311Ile(p.L311I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377524
Start	17660493:17660493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70G>A
AA Mutation	p.Glu24Lys(p.E24K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377524
Start	17705023:17705023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782044601
CDS Mutation	c.1054A>G
AA Mutation	p.Arg352Gly(p.R352G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377524
Start	17688118:17688118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389C>T
AA Mutation	p.Ala130Val(p.A130V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377524
Start	17693261:17693261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484A>C
AA Mutation	p.Lys162Gln(p.K162Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377524
Start	17705723:17705723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1191T>C
Mutation Classification	Silent
Feature Type	Transcript