Mutation

Primary Site >> Stomach Cancer

Gene >> LSS

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46228504:46228504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110C>A
AA Mutation	p.Thr37Asn(p.T37N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46191123:46191123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2180C>T
AA Mutation	p.Ala727Val(p.A727V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46196233:46196233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745641322
CDS Mutation	c.1705C>T
AA Mutation	p.Arg569Trp(p.R569W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46191220:46191220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2083G>A
AA Mutation	p.Val695Ile(p.V695I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46205897:46205897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769378489
CDS Mutation	c.1609G>A
AA Mutation	p.Val537Met(p.V537M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46215718:46215718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.859A>G
AA Mutation	p.Thr287Ala(p.T287A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46215688:46215688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889T>C
AA Mutation	p.Tyr297His(p.Y297H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46196236:46196236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702C>T
AA Mutation	p.Arg568Trp(p.R568W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356396
Start	46195705:46195705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114786885
CDS Mutation	c.1788C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356396
Start	46213794:46213794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766693962
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356396
Start	46216440:46216440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138974013
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356396
Start	46205844:46205844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762730550
CDS Mutation	c.1662G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356396
Start	46215740:46215740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201096401
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356396
Start	46206709:46206709(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1527delG
AA Mutation	p.His510ThrfsTer6(p.H510Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356396
Start	46215736:46215736(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.841delG
AA Mutation	p.Ala281ProfsTer96(p.A281Pfs*96)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356396
Start	46206708:46206709(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1527dupG
AA Mutation	p.His510AlafsTer18(p.H510Afs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript