Mutation

Primary Site >> Stomach Cancer

Gene >> NEURL1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369780
Start	103571703:103571703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.530G>C
AA Mutation	p.Arg177Pro(p.R177P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369780
Start	103585120:103585120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234A>G
AA Mutation	p.Ser412Gly(p.S412G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369780
Start	103570895:103570895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143041435
CDS Mutation	c.109G>A
AA Mutation	p.Val37Ile(p.V37I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369780
Start	103571715:103571715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575166034
CDS Mutation	c.542G>A
AA Mutation	p.Arg181His(p.R181H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369780
Start	103571646:103571646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473C>T
AA Mutation	p.Pro158Leu(p.P158L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369780
Start	103571770:103571770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774528254
CDS Mutation	c.597G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369780
Start	103590201:103590201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771314363
CDS Mutation	c.1554C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000369780
Start	103589557:103589557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1383C>A
AA Mutation	p.Cys461Ter(p.C461*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369780
Start	103571702:103571703(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.529_530insT
AA Mutation	p.Arg177LeufsTer41(p.R177Lfs*41)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript