Mutation

Primary Site >> Stomach Cancer

Gene >> SMARCA4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11033323:11033323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3580G>A
AA Mutation	p.Gly1194Arg(p.G1194R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	10986995:10986995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851G>T
AA Mutation	p.Trp284Leu(p.W284L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	10986955:10986955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769414440
CDS Mutation	c.811G>A
AA Mutation	p.Gly271Arg(p.G271R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11041367:11041367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755455174
CDS Mutation	c.4231C>T
AA Mutation	p.Arg1411Trp(p.R1411W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11024352:11024352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2995G>A
AA Mutation	p.Asp999Asn(p.D999N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11033806:11033806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776672640
CDS Mutation	c.3814G>A
AA Mutation	p.Ala1272Thr(p.A1272T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11003105:11003105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749533909
CDS Mutation	c.1889G>A
AA Mutation	p.Gly630Asp(p.G630D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11010482:11010482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2225T>C
AA Mutation	p.Val742Ala(p.V742A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11024362:11024362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3005C>T
AA Mutation	p.Ala1002Val(p.A1002V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11058797:11058797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4543C>T
AA Mutation	p.Arg1515Cys(p.R1515C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11021866:11021866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2758G>A
AA Mutation	p.Glu920Lys(p.E920K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11024403:11024403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770969438
CDS Mutation	c.3046G>A
AA Mutation	p.Val1016Met(p.V1016M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11023576:11023576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2918G>A
AA Mutation	p.Arg973Gln(p.R973Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11027918:11027918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755069412
CDS Mutation	c.3350C>T
AA Mutation	p.Ala1117Val(p.A1117V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11033317:11033317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3574C>T
AA Mutation	p.Arg1192Cys(p.R1192C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11013018:11013018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2344G>A
AA Mutation	p.Gly782Ser(p.G782S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11033300:11033300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3557C>T
AA Mutation	p.Ala1186Val(p.A1186V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11030751:11030751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3404G>A
AA Mutation	p.Arg1135Gln(p.R1135Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11010423:11010423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2166G>T
AA Mutation	p.Gln722His(p.Q722H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11013017:11013017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2343G>T
AA Mutation	p.Met781Ile(p.M781I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	10986928:10986928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784C>T
AA Mutation	p.Pro262Ser(p.P262S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11024344:11024344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2987T>G
AA Mutation	p.Ile996Ser(p.I996S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11021837:11021837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2729C>T
AA Mutation	p.Thr910Met(p.T910M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	10986266:10986266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433A>T
AA Mutation	p.Met145Leu(p.M145L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	10989388:10989388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1190G>A
AA Mutation	p.Arg397Gln(p.R397Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11033822:11033822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746219091
CDS Mutation	c.3830C>T
AA Mutation	p.Pro1277Leu(p.P1277L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000344626
Start	11033437:11033437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3694G>A
AA Mutation	p.Gly1232Ser(p.G1232S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344626
Start	11027919:11027919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781587481
CDS Mutation	c.3351G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344626
Start	11034985:11034985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372329621
CDS Mutation	c.4023C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344626
Start	11058853:11058853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4599C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344626
Start	11035108:11035108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767883680
CDS Mutation	c.4146A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344626
Start	10996535:10996535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751166438
CDS Mutation	c.1803G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344626
Start	11018975:11018975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368438634
CDS Mutation	c.2457G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344626
Start	11033823:11033823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371304615
CDS Mutation	c.3831G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344626
Start	11021805:11021805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373267815
CDS Mutation	c.2697G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344626
Start	11007979:11007979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2079A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344626
Start	10986949:10986949(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.810delC
AA Mutation	p.Met272CysfsTer31(p.M272Cfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000344626
Start	11027845:11027845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3277C>T
AA Mutation	p.Arg1093Ter(p.R1093*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000344626
Start	10996335:10996420(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1718_1761+42delCTGCCCAGGTCGCCAAGGAGAAAAAGAAGAAAAAGAAAAAGAAGGTGTGCTGGGCCTGGCATGGTGCCCGCCGCGGGTGGGATGGG
Mutation Classification	Splice_Site
Feature Type	Transcript