Mutation

Primary Site >> Stomach Cancer

Gene >> RAI14

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265109
Start	34807815:34807815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769006298
CDS Mutation	c.337G>A
AA Mutation	p.Glu113Lys(p.E113K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265109
Start	34823652:34823652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1810G>A
AA Mutation	p.Ala604Thr(p.A604T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265109
Start	34823865:34823865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2023T>C
AA Mutation	p.Tyr675His(p.Y675H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265109
Start	34795991:34795991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220A>G
AA Mutation	p.Thr74Ala(p.T74A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265109
Start	34830722:34830722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2900A>C
AA Mutation	p.Lys967Thr(p.K967T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265109
Start	34796017:34796017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246A>C
AA Mutation	p.Gln82His(p.Q82H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265109
Start	34824204:34824204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2362T>C
AA Mutation	p.Ser788Pro(p.S788P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265109
Start	34826343:34826343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2663C>T
AA Mutation	p.Ser888Leu(p.S888L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265109
Start	34823780:34823780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761812075
CDS Mutation	c.1938C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265109
Start	34823909:34823909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768901243
CDS Mutation	c.2067C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265109
Start	34823219:34823219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265109
Start	34811062:34811062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265109
Start	34814646:34814646(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.921delT
AA Mutation	p.Phe307LeufsTer20(p.F307Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265109
Start	34813617:34813618(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.816dupA
AA Mutation	p.Arg273ThrfsTer15(p.R273Tfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265109
Start	34821731:34821731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript