Mutation

Primary Site >> Stomach Cancer

Gene >> C3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6712400:6712400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1126G>C
AA Mutation	p.Val376Leu(p.V376L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6707501:6707501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2012G>A
AA Mutation	p.Arg671His(p.R671H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6707236:6707236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2085G>T
AA Mutation	p.Glu695Asp(p.E695D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6697708:6697708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771305132
CDS Mutation	c.2527G>A
AA Mutation	p.Glu843Lys(p.E843K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6680176:6680176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4438T>C
AA Mutation	p.Tyr1480His(p.Y1480H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6678237:6678237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4765A>G
AA Mutation	p.Lys1589Glu(p.K1589E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6702196:6702196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2371A>G
AA Mutation	p.Met791Val(p.M791V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6711118:6711118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348G>T
AA Mutation	p.Gly450Cys(p.G450C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6712375:6712375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1151C>T
AA Mutation	p.Ala384Val(p.A384V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6697686:6697686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2549T>G
AA Mutation	p.Val850Gly(p.V850G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6710724:6710724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1601A>G
AA Mutation	p.Tyr534Cys(p.Y534C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6707193:6707193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2128C>T
AA Mutation	p.Arg710Trp(p.R710W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6707510:6707510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2003G>A
AA Mutation	p.Arg668His(p.R668H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6697424:6697424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2716G>A
AA Mutation	p.Gly906Ser(p.G906S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6712367:6712367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159G>A
AA Mutation	p.Val387Ile(p.V387I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6719333:6719333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145G>A
AA Mutation	p.Ala49Thr(p.A49T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6680214:6680214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4400T>A
AA Mutation	p.Phe1467Tyr(p.F1467Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6697412:6697412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2728G>A
AA Mutation	p.Val910Met(p.V910M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6697672:6697672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765999872
CDS Mutation	c.2563C>T
AA Mutation	p.Arg855Trp(p.R855W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6714011:6714011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754G>C
AA Mutation	p.Glu252Gln(p.E252Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6707486:6707486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139945572
CDS Mutation	c.2027C>T
AA Mutation	p.Thr676Met(p.T676M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6697462:6697462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745503980
CDS Mutation	c.2678C>T
AA Mutation	p.Ser893Leu(p.S893L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6694515:6694515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3070G>A
AA Mutation	p.Ala1024Thr(p.A1024T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6710721:6710721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1604A>G
AA Mutation	p.Tyr535Cys(p.Y535C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6710812:6710812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748352684
CDS Mutation	c.1513C>T
AA Mutation	p.Arg505Cys(p.R505C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6707172:6707172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2149G>A
AA Mutation	p.Gly717Ser(p.G717S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6694489:6694489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3096G>T
AA Mutation	p.Glu1032Asp(p.E1032D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6711022:6711022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149692538
CDS Mutation	c.1444G>A
AA Mutation	p.Ala482Thr(p.A482T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6684806:6684806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3998C>T
AA Mutation	p.Thr1333Ile(p.T1333I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000245907
Start	6710817:6710817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781417846
CDS Mutation	c.1508C>T
AA Mutation	p.Ala503Val(p.A503V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245907
Start	6694528:6694528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749825273
CDS Mutation	c.3057G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245907
Start	6693035:6693035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201084516
CDS Mutation	c.3279C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245907
Start	6684597:6684597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4083C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245907
Start	6718260:6718260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245907
Start	6710774:6710774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1551G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245907
Start	6697772:6697772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2463C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245907
Start	6711188:6711188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138824784
CDS Mutation	c.1278G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000245907
Start	6697470:6697470(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2670delC
AA Mutation	p.Lys891SerfsTer13(p.K891Sfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000245907
Start	6707478:6707478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2035C>T
AA Mutation	p.Arg679Ter(p.R679*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript