Mutation

Primary Site >> Stomach Cancer

Gene >> ATG2B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359933
Start	96311609:96311609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773984669
CDS Mutation	c.3923G>A
AA Mutation	p.Arg1308His(p.R1308H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359933
Start	96347184:96347184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78100888
CDS Mutation	c.320G>A
AA Mutation	p.Arg107His(p.R107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359933
Start	96295140:96295140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563718339
CDS Mutation	c.5246C>T
AA Mutation	p.Thr1749Ile(p.T1749I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359933
Start	96322701:96322701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2575T>A
AA Mutation	p.Ser859Thr(p.S859T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359933
Start	96317194:96317194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3161T>G
AA Mutation	p.Val1054Gly(p.V1054G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359933
Start	96341680:96341680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.766C>T
AA Mutation	p.Pro256Ser(p.P256S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359933
Start	96289715:96289715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5947G>A
AA Mutation	p.Ala1983Thr(p.A1983T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359933
Start	96285961:96285961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6031A>G
AA Mutation	p.Ile2011Val(p.I2011V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359933
Start	96331630:96331630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1476A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359933
Start	96328530:96328530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1980T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359933
Start	96285911:96285911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751217088
CDS Mutation	c.6081C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359933
Start	96332642:96332642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359933
Start	96345318:96345318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359933
Start	96289752:96289752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5910G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000359933
Start	96328537:96328537(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1975-2delA
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000359933
Start	96332303:96332303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1468+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript