Mutation

Primary Site >> Stomach Cancer

Gene >> BACH2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89938218:89938218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1969C>T
AA Mutation	p.Arg657Cys(p.R657C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89951241:89951241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865A>G
AA Mutation	p.Ile289Val(p.I289V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89950787:89950787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1319A>G
AA Mutation	p.Gln440Arg(p.Q440R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89951775:89951775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Cys(p.R111C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89950280:89950280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1826G>T
AA Mutation	p.Arg609Met(p.R609M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89950520:89950520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576225753
CDS Mutation	c.1586C>T
AA Mutation	p.Ala529Val(p.A529V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89932865:89932865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2069C>T
AA Mutation	p.Ser690Leu(p.S690L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89932652:89932652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2282C>T
AA Mutation	p.Ala761Val(p.A761V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89951184:89951184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922G>A
AA Mutation	p.Glu308Lys(p.E308K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	90008753:90008753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92G>A
AA Mutation	p.Arg31Gln(p.R31Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89950449:89950449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1657G>A
AA Mutation	p.Gly553Arg(p.G553R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89951597:89951597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509C>T
AA Mutation	p.Thr170Met(p.T170M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000257749
Start	89950820:89950820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286G>T
AA Mutation	p.Arg429Met(p.R429M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257749
Start	89932735:89932735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2199C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257749
Start	89932615:89932615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150771521
CDS Mutation	c.2319C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257749
Start	89951524:89951524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778129101
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257749
Start	89950579:89950579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257749
Start	89951350:89951350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257749
Start	89950327:89950327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373751160
CDS Mutation	c.1779C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257749
Start	89950519:89950519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201945601
CDS Mutation	c.1587G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257749
Start	89950585:89950585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1521C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257749
Start	89951473:89951473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764844458
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257749
Start	90008731:90008731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257749
Start	89932603:89932603(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2331delC
AA Mutation	p.Gly778AspfsTer19(p.G778Dfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257749
Start	89951848:89951849(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.257dupG
AA Mutation	p.Phe87LeufsTer28(p.F87Lfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	26
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000257749
Start	89932865:89932867(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2067_2069delGTC
AA Mutation	p.Ser690del(p.S690del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript