Mutation

Primary Site >> Stomach Cancer

Gene >> COL4A1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110152466:110152466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766472965
CDS Mutation	c.4796C>T
AA Mutation	p.Ala1599Val(p.A1599V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110150437:110150437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4936A>G
AA Mutation	p.Thr1646Ala(p.T1646A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110162284:110162284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4408G>A
AA Mutation	p.Gly1470Arg(p.G1470R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110176960:110176960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2794C>T
AA Mutation	p.Pro932Ser(p.P932S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110175301:110175301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3115T>G
AA Mutation	p.Leu1039Val(p.L1039V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110177853:110177853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2705C>T
AA Mutation	p.Pro902Leu(p.P902L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110150431:110150431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745486159
CDS Mutation	c.4942T>G
AA Mutation	p.Ser1648Ala(p.S1648A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110181338:110181338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199961869
CDS Mutation	c.2147C>T
AA Mutation	p.Pro716Leu(p.P716L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110163474:110163474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4238C>A
AA Mutation	p.Ala1413Asp(p.A1413D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110178111:110178111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2579C>T
AA Mutation	p.Pro860Leu(p.P860L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110183080:110183080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2008G>A
AA Mutation	p.Gly670Arg(p.G670R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110170574:110170574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3715G>A
AA Mutation	p.Gly1239Arg(p.G1239R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110186424:110186424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1858G>A
AA Mutation	p.Ala620Thr(p.A620T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110183025:110183025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2063G>A
AA Mutation	p.Gly688Asp(p.G688D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110162311:110162311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4381C>T
AA Mutation	p.Pro1461Ser(p.P1461S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110162250:110162250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376607450
CDS Mutation	c.4442G>A
AA Mutation	p.Arg1481Gln(p.R1481Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110176948:110176948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2806G>T
AA Mutation	p.Gly936Cys(p.G936C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110176465:110176465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3017T>G
AA Mutation	p.Leu1006Arg(p.L1006R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110187166:110187166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765386262
CDS Mutation	c.1700C>T
AA Mutation	p.Pro567Leu(p.P567L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110208880:110208880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662G>A
AA Mutation	p.Gly221Asp(p.G221D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110178217:110178217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2473A>G
AA Mutation	p.Lys825Glu(p.K825E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110210193:110210193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488T>G
AA Mutation	p.Leu163Arg(p.L163R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000375820
Start	110179273:110179273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2342G>T
AA Mutation	p.Arg781Ile(p.R781I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110183207:110183207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1967C>A
AA Mutation	p.Ser656Tyr(p.S656Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110152430:110152430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775233741
CDS Mutation	c.4832C>T
AA Mutation	p.Ala1611Val(p.A1611V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110175321:110175321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3095G>A
AA Mutation	p.Gly1032Asp(p.G1032D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110187209:110187209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370670458
CDS Mutation	c.1657G>A
AA Mutation	p.Gly553Ser(p.G553S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000375820
Start	110207420:110207420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779300770
CDS Mutation	c.763G>A
AA Mutation	p.Ala255Thr(p.A255T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110176967:110176967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2787C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110186539:110186539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1743G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110183009:110183009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2079G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110198627:110198627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110174515:110174515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3337C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110152411:110152411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748558670
CDS Mutation	c.4851C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110205518:110205518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110179008:110179008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2373C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110152465:110152465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146638269
CDS Mutation	c.4797G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110192861:110192861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110150432:110150432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115834242
CDS Mutation	c.4941G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110152459:110152459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190097900
CDS Mutation	c.4803C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110162411:110162411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769089749
CDS Mutation	c.4281C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110170575:110170575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377765047
CDS Mutation	c.3714C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110179314:110179314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2301A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375820
Start	110152345:110152345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4917C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375820
Start	110212445:110212445(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.359delC
AA Mutation	p.Pro120GlnfsTer36(p.P120Qfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	46
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375820
Start	110186474:110186474(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1808delC
AA Mutation	p.Pro603LeufsTer199(p.P603Lfs*199)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	47
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375820
Start	110179349:110179349(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2266delG
AA Mutation	p.Glu756ArgfsTer46(p.E756Rfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	48
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375820
Start	110183231:110183231(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1943delC
AA Mutation	p.Pro648LeufsTer154(p.P648Lfs*154)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	49
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375820
Start	110186473:110186474(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1808dupC
AA Mutation	p.Gly604TrpfsTer13(p.G604Wfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	50
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375820
Start	110186518:110186519(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1763dupC
AA Mutation	p.Gly589TrpfsTer11(p.G589Wfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	51
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000375820
Start	110211867:110211867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript