Mutation

Primary Site >> Stomach Cancer

Gene >> ITGBL1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101692669:101692669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762946447
CDS Mutation	c.1100G>A
AA Mutation	p.Arg367His(p.R367H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101598208:101598208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.924G>T
AA Mutation	p.Lys308Asn(p.K308N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101453971:101453971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187T>C
AA Mutation	p.Cys63Arg(p.C63R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101575434:101575434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474C>A
AA Mutation	p.His158Gln(p.H158Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101706833:101706833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210T>G
AA Mutation	p.Cys404Gly(p.C404G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101567750:101567750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368G>T
AA Mutation	p.Gly123Val(p.G123V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101579310:101579310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610A>C
AA Mutation	p.Asn204His(p.N204H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101715626:101715626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765590693
CDS Mutation	c.1457A>G
AA Mutation	p.Glu486Gly(p.E486G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376180
Start	101706764:101706764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1141A>G
AA Mutation	p.Thr381Ala(p.T381A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376180
Start	101452920:101452920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.87G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376180
Start	101583340:101583340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.852T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376180
Start	101567751:101567751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376180
Start	101454072:101454072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376180
Start	101452840:101452840(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.11delC
AA Mutation	p.Pro4GlnfsTer29(p.P4Qfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript