Mutation

Primary Site >> Stomach Cancer

Gene >> ITGAM

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31297835:31297835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1588G>A
AA Mutation	p.Val530Ile(p.V530I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31331208:31331208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3320C>T
AA Mutation	p.Pro1107Leu(p.P1107L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31271944:31271944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762226869
CDS Mutation	c.656C>T
AA Mutation	p.Thr219Met(p.T219M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31271020:31271020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494A>C
AA Mutation	p.Asp165Ala(p.D165A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31321501:31321501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1876T>G
AA Mutation	p.Phe626Val(p.F626V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31273504:31273504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844C>T
AA Mutation	p.Arg282Cys(p.R282C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31297574:31297574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756564190
CDS Mutation	c.1417G>A
AA Mutation	p.Asp473Asn(p.D473N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287497
Start	31331688:31331688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776413889
CDS Mutation	c.3440C>T
AA Mutation	p.Pro1147Leu(p.P1147L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31325338:31325338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2439C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31265821:31265821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.249G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31271969:31271969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41499844
CDS Mutation	c.681G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31321614:31321614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769878845
CDS Mutation	c.1989T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31271957:31271957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31276940:31276940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1104T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31325305:31325305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2406G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287497
Start	31276729:31276729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760185560
CDS Mutation	c.1068C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287497
Start	31271066:31271066(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.545delA
AA Mutation	p.Lys182SerfsTer8(p.K182Sfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287497
Start	31331200:31331200(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3316delC
AA Mutation	p.Leu1106CysfsTer35(p.L1106Cfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000287497
Start	31330313:31330313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3066C>A
AA Mutation	p.Cys1022Ter(p.C1022*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000287497
Start	31325262:31325262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2364-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	21
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000287497
Start	31273451:31273462(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.793_804delCCCTTGGGATAT
AA Mutation	p.Pro265_Tyr268del(p.P265_Y268del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript