Mutation

Primary Site >> Stomach Cancer

Gene >> TUSC3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15623137:15623137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196T>A
AA Mutation	p.Phe66Ile(p.F66I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15748413:15748413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.976T>C
AA Mutation	p.Phe326Leu(p.F326L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15662162:15662162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.574G>A
AA Mutation	p.Val192Ile(p.V192I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15623137:15623137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196T>G
AA Mutation	p.Phe66Val(p.F66V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15623186:15623186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245G>A
AA Mutation	p.Arg82Gln(p.R82Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15659633:15659633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553A>G
AA Mutation	p.Arg185Gly(p.R185G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15540482:15540482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52C>T
AA Mutation	p.Arg18Trp(p.R18W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15662283:15662283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695C>A
AA Mutation	p.Ala232Asp(p.A232D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15662196:15662196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608C>A
AA Mutation	p.Ala203Asp(p.A203D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15623195:15623195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254C>G
AA Mutation	p.Ser85Cys(p.S85C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15650803:15650803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371225890
CDS Mutation	c.415G>A
AA Mutation	p.Val139Ile(p.V139I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15748413:15748413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976T>G
AA Mutation	p.Phe326Val(p.F326V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15650740:15650740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778413040
CDS Mutation	c.352T>G
AA Mutation	p.Tyr118Asp(p.Y118D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15659531:15659531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451T>G
AA Mutation	p.Phe151Val(p.F151V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15743594:15743594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919G>A
AA Mutation	p.Asp307Asn(p.D307N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15623108:15623108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167T>C
AA Mutation	p.Leu56Pro(p.L56P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000503731
Start	15650738:15650738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756614149
CDS Mutation	c.350G>A
AA Mutation	p.Arg117His(p.R117H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000503731
Start	15662290:15662290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.702G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000503731
Start	15748430:15748430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000503731
Start	15743542:15743542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778689006
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000503731
Start	15730705:15730705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838G>T
AA Mutation	p.Glu280Ter(p.E280*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000503731
Start	15623101:15623101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>T
AA Mutation	p.Glu54Ter(p.E54*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript