Mutation

Primary Site >> Stomach Cancer

Gene >> COL14A1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120280009:120280009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775543009
CDS Mutation	c.3556G>A
AA Mutation	p.Ala1186Thr(p.A1186T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120250656:120250656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2642T>C
AA Mutation	p.Ile881Thr(p.I881T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120285947:120285947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4054A>T
AA Mutation	p.Ile1352Phe(p.I1352F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120209827:120209827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1393G>A
AA Mutation	p.Ala465Thr(p.A465T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120197831:120197831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371308409
CDS Mutation	c.613G>A
AA Mutation	p.Asp205Asn(p.D205N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120203786:120203786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759810359
CDS Mutation	c.955G>A
AA Mutation	p.Glu319Lys(p.E319K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120212515:120212515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1535T>C
AA Mutation	p.Val512Ala(p.V512A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120203865:120203865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034T>G
AA Mutation	p.Ile345Ser(p.I345S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120270046:120270046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3085G>A
AA Mutation	p.Ala1029Thr(p.A1029T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120207026:120207026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123C>A
AA Mutation	p.His375Asn(p.H375N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120243981:120243981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556732801
CDS Mutation	c.2452G>A
AA Mutation	p.Val818Ile(p.V818I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120332712:120332712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547704009
CDS Mutation	c.4762C>A
AA Mutation	p.Pro1588Thr(p.P1588T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120226631:120226631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1869A>C
AA Mutation	p.Glu623Asp(p.E623D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120247676:120247676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369592872
CDS Mutation	c.2543C>T
AA Mutation	p.Thr848Met(p.T848M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120243993:120243993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767547791
CDS Mutation	c.2464G>A
AA Mutation	p.Ala822Thr(p.A822T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120243945:120243945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416G>C
AA Mutation	p.Val806Leu(p.V806L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120209831:120209831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1397T>C
AA Mutation	p.Val466Ala(p.V466A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120279977:120279977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369127166
CDS Mutation	c.3524C>T
AA Mutation	p.Ser1175Leu(p.S1175L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000297848
Start	120345561:120345561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372812308
CDS Mutation	c.5075G>A
AA Mutation	p.Arg1692Gln(p.R1692Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120270152:120270152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3191A>C
AA Mutation	p.Lys1064Thr(p.K1064T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120216438:120216438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1685T>C
AA Mutation	p.Ile562Thr(p.I562T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000297848
Start	120247670:120247670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2537G>A
AA Mutation	p.Arg846His(p.R846H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297848
Start	120226661:120226661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1899T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297848
Start	120243986:120243986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763911191
CDS Mutation	c.2457C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297848
Start	120247707:120247707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2574C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297848
Start	120342418:120342418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116831553
CDS Mutation	c.4860G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297848
Start	120278484:120278484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3387T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297848
Start	120279978:120279978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78388021
CDS Mutation	c.3525G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297848
Start	120332714:120332714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561295242
CDS Mutation	c.4764G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297848
Start	120158150:120158150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297848
Start	120209832:120209832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1398G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297848
Start	120244001:120244001(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2476delA
AA Mutation	p.Thr826ProfsTer31(p.T826Pfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000297848
Start	120310024:120310024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4417C>T
AA Mutation	p.Arg1473Ter(p.R1473*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000297848
Start	120289734:120289734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776498858
CDS Mutation	c.4204C>T
AA Mutation	p.Arg1402Ter(p.R1402*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297848
Start	120367231:120367232(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5144dupC
AA Mutation	p.Gly1716TrpfsTer45(p.G1716Wfs*45)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	36
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000297848
Start	120283779:120283779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3967+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	37
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000297848
Start	120225087:120225087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1738-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	38
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000297848
Start	120315588:120315588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4605+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript