Mutation

Primary Site >> Stomach Cancer

Gene >> PSMC3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298852
Start	47420330:47420330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061T>C
AA Mutation	p.Phe354Ser(p.F354S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298852
Start	47422622:47422622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836C>T
AA Mutation	p.Ala279Val(p.A279V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000298852
Start	47424608:47424608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389A>C
AA Mutation	p.Gln130Pro(p.Q130P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298852
Start	47422668:47422668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790G>T
AA Mutation	p.Gly264Cys(p.G264C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298852
Start	47424063:47424063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.574G>A
AA Mutation	p.Asp192Asn(p.D192N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000298852
Start	47425146:47425146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260C>T
AA Mutation	p.Pro87Leu(p.P87L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000298852
Start	47422849:47422849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716C>A
AA Mutation	p.Ala239Asp(p.A239D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298852
Start	47425903:47425903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574933431
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298852
Start	47419145:47419145(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1180delG
AA Mutation	p.Ala394ProfsTer12(p.A394Pfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000298852
Start	47424184:47424184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript