Mutation

Primary Site >> Stomach Cancer

Gene >> ICAM1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264832
Start	10284255:10284255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763586600
CDS Mutation	c.860G>A
AA Mutation	p.Arg287Gln(p.R287Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264832
Start	10284068:10284068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Trp(p.R225W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264832
Start	10284432:10284432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.955A>G
AA Mutation	p.Lys319Glu(p.K319E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264832
Start	10284431:10284431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374392444
CDS Mutation	c.954G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264832
Start	10275003:10275003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264832
Start	10284115:10284115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143689328
CDS Mutation	c.720C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264832
Start	10283503:10283503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779217695
CDS Mutation	c.354G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264832
Start	10271174:10271174(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.19delC
AA Mutation	p.Arg7GlyfsTer40(p.R7Gfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000264832
Start	10284845:10284845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243C>T
AA Mutation	p.Gln415Ter(p.Q415*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript