Mutation

Primary Site >> Stomach Cancer

Gene >> IGHMBP2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255078
Start	68936509:68936509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2029A>G
AA Mutation	p.Ser677Gly(p.S677G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255078
Start	68908157:68908157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269G>A
AA Mutation	p.Gly90Asp(p.G90D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255078
Start	68936797:68936797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754559345
CDS Mutation	c.2317G>A
AA Mutation	p.Gly773Arg(p.G773R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000255078
Start	68906149:68906149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571887680
CDS Mutation	c.167G>A
AA Mutation	p.Arg56His(p.R56H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000255078
Start	68908535:68908535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536962342
CDS Mutation	c.451G>A
AA Mutation	p.Ala151Thr(p.A151T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000255078
Start	68936750:68936750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776484269
CDS Mutation	c.2270G>A
AA Mutation	p.Arg757Gln(p.R757Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000255078
Start	68908228:68908228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340G>C
AA Mutation	p.Val114Leu(p.V114L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000255078
Start	68914901:68914901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139497493
CDS Mutation	c.790C>T
AA Mutation	p.Arg264Cys(p.R264C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000255078
Start	68908605:68908605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521C>G
AA Mutation	p.Ser174Cys(p.S174C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000255078
Start	68933402:68933402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1339G>A
AA Mutation	p.Ala447Thr(p.A447T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000255078
Start	68911499:68911499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768493454
CDS Mutation	c.607G>A
AA Mutation	p.Ala203Thr(p.A203T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255078
Start	68936274:68936274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1794C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255078
Start	68939563:68939563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2814C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255078
Start	68911558:68911558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255078
Start	68908209:68908209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.321C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255078
Start	68937024:68937024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746248057
CDS Mutation	c.2544C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255078
Start	68936517:68936517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2037G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255078
Start	68938279:68938279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2709A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255078
Start	68937054:68937054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2574G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255078
Start	68929335:68929335(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1218delC
AA Mutation	p.Thr407ProfsTer16(p.T407Pfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255078
Start	68936522:68936523(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2045dupG
AA Mutation	p.Gly683ArgfsTer23(p.G683Rfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript