Mutation

Primary Site >> Stomach Cancer

Gene >> USP6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250066
Start	5170554:5170554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749335334
CDS Mutation	c.3593G>T
AA Mutation	p.Arg1198Leu(p.R1198L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250066
Start	5146047:5146047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2192C>A
AA Mutation	p.Pro731His(p.P731H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250066
Start	5138232:5138232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764268758
CDS Mutation	c.1037C>T
AA Mutation	p.Thr346Met(p.T346M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000250066
Start	5138184:5138184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989C>T
AA Mutation	p.Thr330Ile(p.T330I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000250066
Start	5138123:5138123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>T
AA Mutation	p.Arg310Cys(p.R310C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000250066
Start	5132945:5132945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231G>C
AA Mutation	p.Trp77Cys(p.W77C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000250066
Start	5168053:5168053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3158A>G
AA Mutation	p.Tyr1053Cys(p.Y1053C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000250066
Start	5141482:5141482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1556A>C
AA Mutation	p.Lys519Thr(p.K519T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000250066
Start	5130678:5130678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.149T>A
AA Mutation	p.Ile50Asn(p.I50N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000250066
Start	5145562:5145562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2150T>C
AA Mutation	p.Met717Thr(p.M717T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000250066
Start	5138228:5138228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033T>G
AA Mutation	p.Ser345Ala(p.S345A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250066
Start	5147124:5147124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760739101
CDS Mutation	c.2361C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250066
Start	5139274:5139274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1098C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250066
Start	5170618:5170618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3657A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250066
Start	5135867:5135867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250066
Start	5137686:5137686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.861G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250066
Start	5168916:5168916(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3382delG
AA Mutation	p.Asp1128MetfsTer13(p.D1128Mfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250066
Start	5133530:5133530(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.368delA
AA Mutation	p.Asn123ThrfsTer8(p.N123Tfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000250066
Start	5137747:5137747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922C>T
AA Mutation	p.Gln308Ter(p.Q308*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250066
Start	5146095:5146096(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2247dupA
AA Mutation	p.Gln750ThrfsTer9(p.Q750Tfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript