Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LAMC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131041656:131041656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371299880
CDS Mutation	c.1303G>A
AA Mutation	p.Ala435Thr(p.A435T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131009509:131009509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295G>A
AA Mutation	p.Glu99Lys(p.E99K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131026422:131026422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511T>G
AA Mutation	p.Tyr171Asp(p.Y171D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131052932:131052932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146323626
CDS Mutation	c.1906C>T
AA Mutation	p.Arg636Cys(p.R636C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361069
Start	131067205:131067205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2593C>T
AA Mutation	p.Pro865Ser(p.P865S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131057075:131057075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2086C>T
AA Mutation	p.Pro696Ser(p.P696S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131069765:131069765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2984A>G
AA Mutation	p.Asp995Gly(p.D995G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131071515:131071515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149131135
CDS Mutation	c.3101C>T
AA Mutation	p.Thr1034Met(p.T1034M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131052959:131052959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1933C>A
AA Mutation	p.Pro645Thr(p.P645T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131049121:131049121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1621A>C
AA Mutation	p.Thr541Pro(p.T541P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131079186:131079186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146180154
CDS Mutation	c.3815C>T
AA Mutation	p.Ala1272Val(p.A1272V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131068227:131068227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761037173
CDS Mutation	c.2743C>T
AA Mutation	p.Arg915Trp(p.R915W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131045586:131045586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1445G>A
AA Mutation	p.Cys482Tyr(p.C482Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131026366:131026366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773185472
CDS Mutation	c.455G>A
AA Mutation	p.Arg152His(p.R152H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131085548:131085548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4055C>T
AA Mutation	p.Pro1352Leu(p.P1352L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131036210:131036210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750805884
CDS Mutation	c.854C>T
AA Mutation	p.Ala285Val(p.A285V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131039206:131039206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372564761
CDS Mutation	c.1241G>A
AA Mutation	p.Arg414His(p.R414H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131079270:131079270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142459109
CDS Mutation	c.3899C>T
AA Mutation	p.Thr1300Met(p.T1300M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131077296:131077296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3739G>A
AA Mutation	p.Ala1247Thr(p.A1247T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131079156:131079156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3785A>C
AA Mutation	p.Lys1262Thr(p.K1262T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131041677:131041677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1324G>T
AA Mutation	p.Asp442Tyr(p.D442Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131085632:131085632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376347098
CDS Mutation	c.4139C>T
AA Mutation	p.Ala1380Val(p.A1380V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131057109:131057109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2120G>A
AA Mutation	p.Cys707Tyr(p.C707Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131085586:131085586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148481163
CDS Mutation	c.4093G>A
AA Mutation	p.Val1365Ile(p.V1365I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131026450:131026450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778884818
CDS Mutation	c.539G>A
AA Mutation	p.Arg180His(p.R180H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131038953:131038953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138713603
CDS Mutation	c.1066C>T
AA Mutation	p.Arg356Cys(p.R356C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131069777:131069777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2996A>T
AA Mutation	p.Asp999Val(p.D999V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131026343:131026343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131009388:131009388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.174C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131077286:131077286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199639870
CDS Mutation	c.3729C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131036271:131036271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.915G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131057029:131057029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2040G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131056987:131056987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1998A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131069046:131069046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2886C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131036202:131036202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763182921
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131079271:131079271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145960571
CDS Mutation	c.3900G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131085633:131085633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753818876
CDS Mutation	c.4140G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361069
Start	131052553:131052553(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1698delC
AA Mutation	p.Asp568ThrfsTer8(p.D568Tfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361069
Start	131057080:131057080(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2096delG
AA Mutation	p.Gly699ValfsTer185(p.G699Vfs*185)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361069
Start	131066989:131066989(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2382delT
AA Mutation	p.Phe794LeufsTer90(p.F794Lfs*90)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LAMC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131026293:131026293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382T>C
AA Mutation	p.Tyr128His(p.Y128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131041692:131041692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777086759
CDS Mutation	c.1339C>T
AA Mutation	p.Arg447Cys(p.R447C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361069
Start	131045648:131045648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200393760
CDS Mutation	c.1507G>A
AA Mutation	p.Asp503Asn(p.D503N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131072694:131072694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3276G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131032170:131032170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139742340
CDS Mutation	c.804C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131071597:131071597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763614146
CDS Mutation	c.3183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361069
Start	131036310:131036310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377567731
CDS Mutation	c.954C>T
Mutation Classification	Silent
Feature Type	Transcript