Mutation

Primary Site >> Stomach Cancer

Gene >> GSDMC

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276708
Start	129776200:129776200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306A>C
AA Mutation	p.Glu102Asp(p.E102D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276708
Start	129750035:129750035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168T>A
AA Mutation	p.Phe390Ile(p.F390I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000276708
Start	129752820:129752820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.722A>G
AA Mutation	p.Glu241Gly(p.E241G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000276708
Start	129776115:129776115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.391G>A
AA Mutation	p.Asp131Asn(p.D131N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000276708
Start	129777568:129777568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771002121
CDS Mutation	c.20G>A
AA Mutation	p.Arg7His(p.R7H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000276708
Start	129776109:129776109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397C>A
AA Mutation	p.Gln133Lys(p.Q133K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000276708
Start	129748716:129748716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1312T>G
AA Mutation	p.Phe438Val(p.F438V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000276708
Start	129749514:129749514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1225T>G
AA Mutation	p.Phe409Val(p.F409V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000276708
Start	129777452:129777452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140640562
CDS Mutation	c.136C>T
AA Mutation	p.Arg46Cys(p.R46C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000276708
Start	129751556:129751556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929A>T
AA Mutation	p.Glu310Val(p.E310V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000276708
Start	129751542:129751542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943A>G
AA Mutation	p.Asn315Asp(p.N315D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000276708
Start	129776104:129776104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402A>C
AA Mutation	p.Lys134Asn(p.K134N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000276708
Start	129752698:129752698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.844G>A
AA Mutation	p.Glu282Lys(p.E282K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000276708
Start	129777387:129777387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201G>T
AA Mutation	p.Glu67Asp(p.E67D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000276708
Start	129777487:129777487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.101G>A
AA Mutation	p.Arg34His(p.R34H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276708
Start	129777372:129777372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276708
Start	129748510:129748510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1518T>C
Mutation Classification	Silent
Feature Type	Transcript