Mutation

Primary Site >> Stomach Cancer

Gene >> MUC6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1025193:1025193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2974C>A
AA Mutation	p.Arg992Ser(p.R992S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1013590:1013590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7186T>C
AA Mutation	p.Cys2396Arg(p.C2396R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1023628:1023628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373492122
CDS Mutation	c.3407C>T
AA Mutation	p.Thr1136Met(p.T1136M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1016179:1016179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6622A>T
AA Mutation	p.Ile2208Phe(p.I2208F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1016190:1016190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6611C>T
AA Mutation	p.Ala2204Val(p.A2204V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1026380:1026380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2493C>A
AA Mutation	p.Phe831Leu(p.F831L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1027310:1027310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2189T>C
AA Mutation	p.Phe730Ser(p.F730S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1027763:1027763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779356933
CDS Mutation	c.1903G>A
AA Mutation	p.Ala635Thr(p.A635T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1017006:1017006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5795C>T
AA Mutation	p.Pro1932Leu(p.P1932L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1027455:1027455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2044C>A
AA Mutation	p.Leu682Met(p.L682M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1031856:1031856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148640037
CDS Mutation	c.313G>A
AA Mutation	p.Val105Ile(p.V105I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1031906:1031906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547156930
CDS Mutation	c.263G>A
AA Mutation	p.Arg88Gln(p.R88Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1016104:1016104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373036328
CDS Mutation	c.6697G>A
AA Mutation	p.Val2233Met(p.V2233M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1025025:1025025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367909154
CDS Mutation	c.3044C>T
AA Mutation	p.Thr1015Met(p.T1015M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1019478:1019478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752301400
CDS Mutation	c.3827C>T
AA Mutation	p.Thr1276Met(p.T1276M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1024040:1024040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3289G>A
AA Mutation	p.Asp1097Asn(p.D1097N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1016404:1016404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6397C>T
AA Mutation	p.Pro2133Ser(p.P2133S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1033061:1033061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.67T>A
AA Mutation	p.Ser23Thr(p.S23T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1016248:1016248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6553A>C
AA Mutation	p.Thr2185Pro(p.T2185P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1019287:1019287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4018A>G
AA Mutation	p.Ser1340Gly(p.S1340G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1020720:1020720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3604C>T
AA Mutation	p.Pro1202Ser(p.P1202S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1024088:1024088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3241T>A
AA Mutation	p.Tyr1081Asn(p.Y1081N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1031855:1031855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314T>C
AA Mutation	p.Val105Ala(p.V105A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1027331:1027331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2168G>A
AA Mutation	p.Cys723Tyr(p.C723Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1025196:1025196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201406450
CDS Mutation	c.2971G>A
AA Mutation	p.Ala991Thr(p.A991T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1027176:1027176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201174742
CDS Mutation	c.2249G>A
AA Mutation	p.Arg750Gln(p.R750Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1025310:1025310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527440972
CDS Mutation	c.2857G>A
AA Mutation	p.Val953Met(p.V953M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1025234:1025234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2933T>G
AA Mutation	p.Leu978Arg(p.L978R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1016092:1016092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6709C>A
AA Mutation	p.Pro2237Thr(p.P2237T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1019473:1019473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776231978
CDS Mutation	c.3832G>A
AA Mutation	p.Val1278Ile(p.V1278I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1023607:1023607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3428G>A
AA Mutation	p.Gly1143Asp(p.G1143D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1015989:1015989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6812C>T
AA Mutation	p.Ser2271Leu(p.S2271L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1028329:1028329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762339289
CDS Mutation	c.1650C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1018712:1018712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4089T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1016369:1016369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759446051
CDS Mutation	c.6432T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1026404:1026404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2469C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1016108:1016108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6693T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1025844:1025844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753380098
CDS Mutation	c.2760C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1018685:1018685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4116A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1027755:1027755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1911C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1026075:1026075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2613C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1021246:1021246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779473001
CDS Mutation	c.3558C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1031986:1031986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769255270
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1016417:1016417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6384C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1017061:1017061(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5740delA
AA Mutation	p.Thr1914LeufsTer71(p.T1914Lfs*71)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	46
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1033016:1033017(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.111_112delGA
AA Mutation	p.Gln37HisfsTer120(p.Q37Hfs*120)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	47
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1025853:1025859(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2745_2751delCATCTGT
AA Mutation	p.Ile916GlyfsTer40(p.I916Gfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	48
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1019329:1019329(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3976delC
AA Mutation	p.Arg1326GlyfsTer4(p.R1326Gfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	49
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1018609:1018612(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4189_4192delTACA
AA Mutation	p.Tyr1397GlnfsTer58(p.Y1397Qfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	50
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1018736:1018742(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4059_4065delAACAACG
AA Mutation	p.Thr1354ProfsTer100(p.T1354Pfs*100)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	51
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1016296:1016305(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6496_6505delGTGTCCGCCC
AA Mutation	p.Val2166ProfsTer7(p.V2166Pfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	52
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1024987:1024988(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3081_3082delGG
AA Mutation	p.Leu1027PhefsTer66(p.L1027Ffs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1020714:1020721(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3603_3610delGCCGCAGC
AA Mutation	p.Pro1202ThrfsTer39(p.P1202Tfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	54
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1016374:1016377(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6424_6427delTCTT
AA Mutation	p.Ser2142LeufsTer33(p.S2142Lfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	55
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1016229:1016241(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6560_6572delCCACGACTGCATC
AA Mutation	p.Pro2187GlnfsTer51(p.P2187Qfs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	56
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1015927:1015927(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6874delG
AA Mutation	p.Val2292Ter(p.V2292*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	57
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1027310:1027319(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2180_2189delGTTACAAGTT
AA Mutation	p.Gly727AlafsTer22(p.G727Afs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	58
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000421673
Start	1016155:1016156(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6645_6646insTGAAATCA
AA Mutation	p.Ile2216Ter(p.I2216*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	59
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000421673
Start	1016157:1016158(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6643_6644insTTGATTTTTGAACCTTTATAATAAGT
AA Mutation	p.Thr2215IlefsTer4(p.T2215Ifs*4)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	60
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1026400:1026401(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2472dupC
AA Mutation	p.Glu825ArgfsTer6(p.E825Rfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	61
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421673
Start	1016000:1016001(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6796_6800dupTCTCA
AA Mutation	p.Gln2267HisfsTer28(p.Q2267Hfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	62
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000421673
Start	1029229:1029230(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1273dupC
AA Mutation	p.Gln425ProfsTer119(p.Q425Pfs*119)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	63
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000421673
Start	1023648:1023681(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3383-29_3387delCCACCAGCTGACAGCTCCCTTCCTCCCAGCCATC
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	64
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000421673
Start	1017746:1017748(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5053_5055delTTA
AA Mutation	p.Leu1685del(p.L1685del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript