Mutation

Primary Site >> Stomach Cancer

Gene >> SMARCC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47678273:47678273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759334676
CDS Mutation	c.1496G>A
AA Mutation	p.Arg499His(p.R499H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47729087:47729087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584T>G
AA Mutation	p.Phe195Cys(p.F195C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47701358:47701358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1085A>T
AA Mutation	p.Asp362Val(p.D362V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47678297:47678297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1472G>A
AA Mutation	p.Arg491Gln(p.R491Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47675509:47675509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1805G>A
AA Mutation	p.Arg602His(p.R602H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47738072:47738072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440G>A
AA Mutation	p.Arg147His(p.R147H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47689407:47689407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776988969
CDS Mutation	c.1243A>G
AA Mutation	p.Thr415Ala(p.T415A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47693290:47693290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1176G>T
AA Mutation	p.Lys392Asn(p.K392N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47610294:47610294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760989176
CDS Mutation	c.2815C>T
AA Mutation	p.Arg939Cys(p.R939C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47745984:47745984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325T>C
AA Mutation	p.Phe109Leu(p.F109L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47590794:47590794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3087G>A
AA Mutation	p.Met1029Ile(p.M1029I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000254480
Start	47706446:47706446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003A>G
AA Mutation	p.Thr335Ala(p.T335A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254480
Start	47588275:47588275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3252A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254480
Start	47610292:47610292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2817C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254480
Start	47610232:47610232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2877A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254480
Start	47636069:47636069(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2444delA
AA Mutation	p.Asn815IlefsTer10(p.N815Ifs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000254480
Start	47610252:47610252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2857C>T
AA Mutation	p.Arg953Ter(p.R953*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000254480
Start	47670688:47670688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1869G>A
AA Mutation	p.Trp623Ter(p.W623*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254480
Start	47636068:47636069(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2444dupA
AA Mutation	p.Asn815LysfsTer2(p.N815Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254480
Start	47680457:47680458(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1436dupA
AA Mutation	p.Asn479LysfsTer18(p.N479Kfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	21
Mutation Consequence	splice_donor_variant;intron_variant
Transcription ID	ENST00000254480
Start	47689375:47689386(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1263+1_1263+12delGTAACAATTCAG
Mutation Classification	Splice_Site
Feature Type	Transcript