Mutation

Primary Site >> Stomach Cancer

Gene >> AHSG

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000411641
Start	186613170:186613170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29T>G
AA Mutation	p.Leu10Arg(p.L10R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000411641
Start	186613265:186613265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124C>A
AA Mutation	p.Leu42Met(p.L42M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000411641
Start	186620659:186620659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833C>A
AA Mutation	p.Pro278His(p.P278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000411641
Start	186620836:186620836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755858937
CDS Mutation	c.1010G>A
AA Mutation	p.Arg337Gln(p.R337Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000411641
Start	186613321:186613321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180G>C
AA Mutation	p.Leu60Phe(p.L60F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000411641
Start	186617218:186617218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000411641
Start	186615774:186615774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141353291
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000411641
Start	186620664:186620665(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.842dupC
AA Mutation	p.Pro282SerfsTer65(p.P282Sfs*65)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000411641
Start	186617185:186617185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.410-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript