Mutation

Primary Site >> Stomach Cancer

Gene >> DLC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13091340:13091340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3833C>G
AA Mutation	p.Ala1278Gly(p.A1278G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13088622:13088622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4157T>C
AA Mutation	p.Leu1386Pro(p.L1386P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13099697:13099697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2640C>G
AA Mutation	p.Asp880Glu(p.D880E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13499912:13499912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368389913
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Cys(p.R54C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13499161:13499161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911A>C
AA Mutation	p.Asn304Thr(p.N304T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13499329:13499329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777668661
CDS Mutation	c.743G>T
AA Mutation	p.Ser248Ile(p.S248I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13100683:13100683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1654G>C
AA Mutation	p.Glu552Gln(p.E552Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13401480:13401480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150701452
CDS Mutation	c.1163G>A
AA Mutation	p.Arg388Gln(p.R388Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13499554:13499554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518C>A
AA Mutation	p.Ala173Glu(p.A173E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13099623:13099623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2714A>C
AA Mutation	p.Glu905Ala(p.E905A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13100374:13100374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1963G>T
AA Mutation	p.Gly655Cys(p.G655C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13099423:13099423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2914A>G
AA Mutation	p.Asn972Asp(p.N972D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13090446:13090446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747060194
CDS Mutation	c.3880C>T
AA Mutation	p.Arg1294Cys(p.R1294C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13092784:13092784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3568A>T
AA Mutation	p.Ile1190Phe(p.I1190F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13100164:13100164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2173A>G
AA Mutation	p.Asn725Asp(p.N725D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13099658:13099658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2679C>A
AA Mutation	p.Asp893Glu(p.D893E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13100073:13100073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201189821
CDS Mutation	c.2264C>T
AA Mutation	p.Thr755Met(p.T755M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13100193:13100193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2144A>G
AA Mutation	p.Glu715Gly(p.E715G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13499221:13499221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851G>A
AA Mutation	p.Cys284Tyr(p.C284Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13499992:13499992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11990333
CDS Mutation	c.80G>A
AA Mutation	p.Arg27His(p.R27H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13088698:13088698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767802518
CDS Mutation	c.4081G>A
AA Mutation	p.Glu1361Lys(p.E1361K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13499524:13499524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548T>G
AA Mutation	p.Val183Gly(p.V183G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13115616:13115616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390G>A
AA Mutation	p.Gly464Ser(p.G464S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13091352:13091352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3821C>G
AA Mutation	p.Ala1274Gly(p.A1274G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13102808:13102808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1548T>G
AA Mutation	p.Ile516Met(p.I516M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000276297
Start	13100574:13100574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762870802
CDS Mutation	c.1763G>A
AA Mutation	p.Arg588His(p.R588H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13100621:13100621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752727723
CDS Mutation	c.1716G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13100279:13100279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372344109
CDS Mutation	c.2058G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13086340:13086340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4416C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13099469:13099469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756567103
CDS Mutation	c.2868C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13099931:13099931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2406A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13091342:13091342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747673048
CDS Mutation	c.3831C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13499679:13499679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13100252:13100252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148579135
CDS Mutation	c.2085C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13099625:13099625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749152245
CDS Mutation	c.2712C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13499769:13499769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.303A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13099766:13099766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745723621
CDS Mutation	c.2571C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13499552:13499552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276297
Start	13099601:13099601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2736C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000276297
Start	13100488:13100488(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1849delC
AA Mutation	p.Arg617GlyfsTer37(p.R617Gfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000276297
Start	13110772:13110772(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1472delT
AA Mutation	p.Leu491TrpfsTer13(p.L491Wfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000276297
Start	13099850:13099850(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2487delC
AA Mutation	p.Ser830ArgfsTer7(p.S830Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript