Mutation

Primary Site >> Stomach Cancer

Gene >> MUC4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195774186:195774186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770422854
CDS Mutation	c.13063C>T
AA Mutation	p.Arg4355Cys(p.R4355C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195747199:195747199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16216A>G
AA Mutation	p.Asn5406Asp(p.N5406D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195759159:195759159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369127921
CDS Mutation	c.14951C>T
AA Mutation	p.Thr4984Met(p.T4984M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195762102:195762102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14497A>G
AA Mutation	p.Thr4833Ala(p.T4833A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195769029:195769029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13522T>G
AA Mutation	p.Phe4508Val(p.F4508V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195778371:195778371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12875C>T
AA Mutation	p.Ser4292Phe(p.S4292F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195788744:195788744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2836G>C
AA Mutation	p.Gly946Arg(p.G946R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195784283:195784283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7297C>T
AA Mutation	p.Leu2433Phe(p.L2433F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195790190:195790190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781336737
CDS Mutation	c.1390C>T
AA Mutation	p.Arg464Trp(p.R464W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195765347:195765347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13721G>C
AA Mutation	p.Trp4574Ser(p.W4574S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000463781
Start	195771653:195771653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13241A>G
AA Mutation	p.Gln4414Arg(p.Q4414R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195747240:195747240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754106095
CDS Mutation	c.16175G>A
AA Mutation	p.Arg5392His(p.R5392H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195769067:195769067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13484A>G
AA Mutation	p.Asp4495Gly(p.D4495G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195753134:195753134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771793916
CDS Mutation	c.15425A>G
AA Mutation	p.Gln5142Arg(p.Q5142R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195752417:195752417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.15538C>T
AA Mutation	p.Leu5180Phe(p.L5180F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195791380:195791380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200A>T
AA Mutation	p.Asn67Ile(p.N67I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195789102:195789102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2478G>T
AA Mutation	p.Glu826Asp(p.E826D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195789532:195789532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199528786
CDS Mutation	c.2048C>T
AA Mutation	p.Pro683Leu(p.P683L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195757290:195757290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.15025C>T
AA Mutation	p.Pro5009Ser(p.P5009S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195788950:195788950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2630C>G
AA Mutation	p.Ser877Cys(p.S877C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195789100:195789100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750131166
CDS Mutation	c.2480C>T
AA Mutation	p.Thr827Met(p.T827M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195790523:195790523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057T>G
AA Mutation	p.Leu353Val(p.L353V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195771689:195771689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13205C>T
AA Mutation	p.Ala4402Val(p.A4402V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195788989:195788989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372862585
CDS Mutation	c.2591C>T
AA Mutation	p.Ala864Val(p.A864V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195754276:195754276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754721080
CDS Mutation	c.15265G>A
AA Mutation	p.Val5089Ile(p.V5089I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195781363:195781363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10217C>T
AA Mutation	p.Thr3406Ile(p.T3406I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195781508:195781508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10072G>A
AA Mutation	p.Ala3358Thr(p.A3358T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195788926:195788926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752700892
CDS Mutation	c.2654C>T
AA Mutation	p.Pro885Leu(p.P885L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195779310:195779310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12270C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195769084:195769084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373895108
CDS Mutation	c.13467C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195754352:195754352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528677619
CDS Mutation	c.15189C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195770294:195770294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368770871
CDS Mutation	c.13320C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195789204:195789204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2376C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195759158:195759158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757528643
CDS Mutation	c.14952G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195788793:195788793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561801234
CDS Mutation	c.2787C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195747314:195747314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16101C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195765412:195765412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771963259
CDS Mutation	c.13656A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195790056:195790056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1524A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195778379:195778379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12867C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195774205:195774205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13044C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000463781
Start	195761501:195761501(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.14597delT
AA Mutation	p.Phe4866SerfsTer5(p.F4866Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000463781
Start	195761524:195761525(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.14573dupC
AA Mutation	p.Gly4859ArgfsTer4(p.G4859Rfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript