Mutation

Primary Site >> Stomach Cancer

Gene >> ACIN1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23061345:23061345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3551G>T
AA Mutation	p.Arg1184Leu(p.R1184L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23080301:23080301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs12589748
CDS Mutation	c.1208C>T
AA Mutation	p.Ala403Val(p.A403V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23081833:23081833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614A>C
AA Mutation	p.Lys205Thr(p.K205T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23059156:23059156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4018C>T
AA Mutation	p.Arg1340Cys(p.R1340C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23061088:23061088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3695G>T
AA Mutation	p.Ser1232Ile(p.S1232I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23063030:23063030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2956A>C
AA Mutation	p.Lys986Gln(p.K986Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23061417:23061417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754494408
CDS Mutation	c.3479G>T
AA Mutation	p.Arg1160Leu(p.R1160L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23063027:23063027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2959T>G
AA Mutation	p.Ser987Ala(p.S987A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23079737:23079737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1772C>T
AA Mutation	p.Ser591Leu(p.S591L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23095145:23095145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142G>T
AA Mutation	p.Ala48Ser(p.A48S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23079717:23079717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772662866
CDS Mutation	c.1792A>G
AA Mutation	p.Ser598Gly(p.S598G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23059206:23059206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761845612
CDS Mutation	c.3968G>A
AA Mutation	p.Arg1323His(p.R1323H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262710
Start	23080149:23080149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776587268
CDS Mutation	c.1360C>T
AA Mutation	p.Pro454Ser(p.P454S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262710
Start	23061524:23061524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140303626
CDS Mutation	c.3372G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262710
Start	23062470:23062470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3111C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262710
Start	23062506:23062506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3075A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262710
Start	23059178:23059178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3996A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262710
Start	23090094:23090094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762302314
CDS Mutation	c.498A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262710
Start	23080170:23080170(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1339delG
AA Mutation	p.Ala447LeufsTer19(p.A447Lfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262710
Start	23069567:23069567(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2348delA
AA Mutation	p.Asn783MetfsTer89(p.N783Mfs*89)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262710
Start	23062963:23062963(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3023delG
AA Mutation	p.Gly1008AlafsTer18(p.G1008Afs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262710
Start	23064474:23064474(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2497delG
AA Mutation	p.Val833CysfsTer39(p.V833Cfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript