Mutation

Primary Site >> Stomach Cancer

Gene >> MAGEC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141905537:141905537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133G>A
AA Mutation	p.Asp45Asn(p.D45N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907028:141907028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1624T>C
AA Mutation	p.Ser542Pro(p.S542P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141905591:141905591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187T>C
AA Mutation	p.Ser63Pro(p.S63P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907257:141907257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1853G>T
AA Mutation	p.Gly618Val(p.G618V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141908542:141908542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753057119
CDS Mutation	c.3138A>C
AA Mutation	p.Lys1046Asn(p.K1046N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141906800:141906800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1396A>C
AA Mutation	p.Thr466Pro(p.T466P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141908298:141908298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2894T>A
AA Mutation	p.Leu965Gln(p.L965Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907396:141907396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1992G>T
AA Mutation	p.Gln664His(p.Q664H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141908544:141908544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3140T>G
AA Mutation	p.Val1047Gly(p.V1047G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907820:141907820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416G>T
AA Mutation	p.Ala806Ser(p.A806S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907215:141907215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1811A>T
AA Mutation	p.Asp604Val(p.D604V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141908514:141908514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3110T>A
AA Mutation	p.Phe1037Tyr(p.F1037Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141906450:141906450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046C>T
AA Mutation	p.Thr349Ile(p.T349I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141908355:141908355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2951C>A
AA Mutation	p.Ser984Tyr(p.S984Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907465:141907465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2061T>G
AA Mutation	p.Asp687Glu(p.D687E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907264:141907264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1860A>T
AA Mutation	p.Glu620Asp(p.E620D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907513:141907513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2109C>A
AA Mutation	p.Asp703Glu(p.D703E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907646:141907646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2242T>A
AA Mutation	p.Ser748Thr(p.S748T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907242:141907242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1838A>C
AA Mutation	p.Gln613Pro(p.Q613P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141908687:141908687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147835720
CDS Mutation	c.3283G>A
AA Mutation	p.Val1095Ile(p.V1095I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141905499:141905499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95A>G
AA Mutation	p.Gln32Arg(p.Q32R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907517:141907517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2113C>A
AA Mutation	p.Leu705Met(p.L705M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141908568:141908568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762692975
CDS Mutation	c.3164A>G
AA Mutation	p.Glu1055Gly(p.E1055G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141907842:141907842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2438C>A
AA Mutation	p.Pro813His(p.P813H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141908451:141908451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3047A>G
AA Mutation	p.Glu1016Gly(p.E1016G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141908720:141908720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3316G>A
AA Mutation	p.Ala1106Thr(p.A1106T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000285879
Start	141905540:141905540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761310657
CDS Mutation	c.136G>A
AA Mutation	p.Asp46Asn(p.D46N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285879
Start	141908296:141908296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2892C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285879
Start	141908050:141908050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2646A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285879
Start	141906295:141906295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285879
Start	141905539:141905539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781697121
CDS Mutation	c.135C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285879
Start	141906862:141906862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1458C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285879
Start	141908212:141908212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2808G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285879
Start	141905470:141905470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285879
Start	141907429:141907429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771561079
CDS Mutation	c.2025T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000285879
Start	141906054:141906054(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.653delC
AA Mutation	p.Pro218LeufsTer20(p.P218Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000285879
Start	141907600:141907600(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2200delG
AA Mutation	p.Glu734ArgfsTer11(p.E734Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000285879
Start	141908786:141908786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3382G>T
AA Mutation	p.Glu1128Ter(p.E1128*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript