Mutation

Primary Site >> Stomach Cancer

Gene >> ZNF418

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396147
Start	57926844:57926844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773424528
CDS Mutation	c.1337G>A
AA Mutation	p.Arg446Gln(p.R446Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396147
Start	57926955:57926955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773985943
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409Gln(p.R409Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396147
Start	57926787:57926787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1394G>A
AA Mutation	p.Gly465Asp(p.G465D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396147
Start	57927004:57927004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177A>G
AA Mutation	p.Thr393Ala(p.T393A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396147
Start	57927048:57927048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1133G>A
AA Mutation	p.Cys378Tyr(p.C378Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396147
Start	57926159:57926159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2022T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396147
Start	57926783:57926783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1398G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396147
Start	57927803:57927803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141826842
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396147
Start	57926366:57926366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746811618
CDS Mutation	c.1815G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396147
Start	57927950:57927950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396147
Start	57927920:57927920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000396147
Start	57928006:57928006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.175A>T
AA Mutation	p.Lys59Ter(p.K59*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396147
Start	57927508:57927509(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.672dupT
AA Mutation	p.Pro225SerfsTer3(p.P225Sfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript