Mutation

Primary Site >> Stomach Cancer

Gene >> DSG2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31542737:31542737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2219T>C
AA Mutation	p.Met740Thr(p.M740T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31542823:31542823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371146201
CDS Mutation	c.2305G>A
AA Mutation	p.Glu769Lys(p.E769K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31536273:31536273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759612298
CDS Mutation	c.1495C>A
AA Mutation	p.Leu499Met(p.L499M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31536421:31536421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551034751
CDS Mutation	c.1643G>A
AA Mutation	p.Arg548His(p.R548H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31541280:31541280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1967C>A
AA Mutation	p.Pro656His(p.P656H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31546610:31546610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3224C>T
AA Mutation	p.Thr1075Met(p.T1075M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31542775:31542775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2257G>A
AA Mutation	p.Ala753Thr(p.A753T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261590
Start	31541233:31541233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775642244
CDS Mutation	c.1920C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261590
Start	31521236:31521236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261590
Start	31531070:31531070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1098T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261590
Start	31542729:31542729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs74578148
CDS Mutation	c.2211C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261590
Start	31545990:31545990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2604T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261590
Start	31545914:31545914(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2533delA
AA Mutation	p.Ile845Ter(p.I845*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261590
Start	31536403:31536403(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1629delA
AA Mutation	p.Lys543AsnfsTer4(p.K543Nfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261590
Start	31520955:31520956(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.375dupT
AA Mutation	p.Leu126SerfsTer23(p.L126Sfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript