Mutation

Primary Site >> Stomach Cancer

Gene >> MMP2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219070
Start	55502808:55502808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756048527
CDS Mutation	c.1799C>T
AA Mutation	p.Pro600Leu(p.P600L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219070
Start	55485643:55485643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698G>A
AA Mutation	p.Cys233Tyr(p.C233Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000219070
Start	55491801:55491801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1181G>A
AA Mutation	p.Gly394Glu(p.G394E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219070
Start	55498363:55498363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1684C>T
AA Mutation	p.Pro562Ser(p.P562S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000219070
Start	55485365:55485365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.596C>T
AA Mutation	p.Thr199Ile(p.T199I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000219070
Start	55493185:55493185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1364C>A
AA Mutation	p.Thr455Asn(p.T455N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000219070
Start	55484071:55484071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436C>T
AA Mutation	p.Arg146Cys(p.R146C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000219070
Start	55489788:55489788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555030156
CDS Mutation	c.1144G>A
AA Mutation	p.Asp382Asn(p.D382N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55484091:55484091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371188032
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55493255:55493255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754804742
CDS Mutation	c.1434C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55488679:55488679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561800947
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55498410:55498410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55479575:55479575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.96G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55482962:55482962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.207G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55485306:55485306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151071926
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55491844:55491844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55479605:55479605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55488565:55488565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760006274
CDS Mutation	c.855C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55489808:55489808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1164C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55483022:55483022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55485704:55485704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148801200
CDS Mutation	c.759C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219070
Start	55479596:55479596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139082366
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000219070
Start	55493194:55493194(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1377delC
AA Mutation	p.Thr460ArgfsTer38(p.T460Rfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000219070
Start	55484116:55484116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481C>T
AA Mutation	p.Arg161Ter(p.R161*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript