Mutation

Primary Site >> Liver Cancer

Gene >> MUC4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195781125:195781125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10455C>A
AA Mutation	p.His3485Gln(p.H3485Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195781085:195781085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10495A>T
AA Mutation	p.Thr3499Ser(p.T3499S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195781247:195781247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554580122
CDS Mutation	c.10333A>G
AA Mutation	p.Ser3445Gly(p.S3445G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195781075:195781075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10505C>A
AA Mutation	p.Thr3502Asn(p.T3502N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195785255:195785255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6325C>A
AA Mutation	p.His2109Asn(p.H2109N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195783182:195783182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8398C>A
AA Mutation	p.Pro2800Thr(p.P2800T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195774205:195774205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13044C>G
AA Mutation	p.Phe4348Leu(p.F4348L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195747220:195747220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772843001
CDS Mutation	c.16195G>A
AA Mutation	p.Ala5399Thr(p.A5399T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195786058:195786058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5522T>A
AA Mutation	p.Leu1841His(p.L1841H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000463781
Start	195786794:195786794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776638001
CDS Mutation	c.4786G>C
AA Mutation	p.Gly1596Arg(p.G1596R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195786195:195786195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5385C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195749051:195749051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752078558
CDS Mutation	c.15885G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195788814:195788814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2766C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195751003:195751003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542498469
CDS Mutation	c.15757C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195747326:195747326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16089C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195780417:195780417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11163A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195781074:195781074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10506C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195787983:195787983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3597C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195790449:195790449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1131C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195779247:195779247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12333G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195782460:195782460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9120G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195779775:195779775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11805C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195786306:195786306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5274C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463781
Start	195785298:195785298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6282C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000463781
Start	195783072:195783075(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.8505_8508delCACC
AA Mutation	p.Thr2836SerfsTer167(p.T2836Sfs*167)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000463781
Start	195782751:195782752(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.8828_8829insGCCTCTTCCTGTCACCAGCCTTTCCTCAGTATCCACAGGTCACGCCA
AA Mutation	p.Asp2949SerfsTer71(p.D2949Sfs*71)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000463781
Start	195783224:195783225(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.8355_8356insGCTGTCACCGACACTTCCTCAGTATCCACAGGTCACGC
AA Mutation	p.His2786AlafsTer231(p.H2786Afs*231)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	28
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000463781
Start	195778959:195779102(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.12478_12621delTCTCTTCCTGTCACCGACGCTTCCTCAGTGTCCACAGGTCACGGCACCCCTCTTCCTGTCACCAGCACTTCCTCAGCATCCACAGGTGACACCACCCCTCTTCCTGTCACCGACACTTCCTCAGCATCCACAGGTCACGCCACC
AA Mutation	p.Ser4160_Thr4207del(p.S4160_T4207del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

ID	29
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000463781
Start	195781031:195781032(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.10548_10549insGACACCACGACTCTTCCTGTCACCGACACTTCCTCAGTATCCACAGGTCACGCCACCCCTCTTCCTGTCACCAGCTTTTCCTCAGTATCCACAGGTGACACCACCCCTCTTCCTGTCACCGACGCTTCCTCGGCATCCACCGGT
AA Mutation	p.Gly3516_His3517insAspThrThrThrLeuProValThrAspThrSerSerValSerThrGlyHisAlaThrProLeuProValThrSerPheSerSerValSerThrGlyAspThrThrProLeuProValThrAspAlaSerSerAlaSerThrGly(p.G3516_H3517insDTTTLPVTDTSSVSTGHATPLPVTSFSSVSTGDTTPLPVTDASSASTG)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

ID	30
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000463781
Start	195781028:195781029(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.10551_10552insACCACGACTCTTCCTGTCACCGACACTTCCTCAGTATCCACAGGTCACGCCACCCCTCTTCCTGTCACCAGCTTTTCCTCAGTATCCACAGGTGACACCACCCCTCTTCCTGTCACCGACGCTTCCTCGGCATCCACCGGTCAC
AA Mutation	p.His3517_Ala3518insThrThrThrLeuProValThrAspThrSerSerValSerThrGlyHisAlaThrProLeuProValThrSerPheSerSerValSerThrGlyAspThrThrProLeuProValThrAspAlaSerSerAlaSerThrGlyHis(p.H3517_A3518insTTTLPVTDTSSVSTGHATPLPVTSFSSVSTGDTTPLPVTDASSASTGH)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

ID	31
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000463781
Start	195782660:195782661(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.8919_8920insACCACCCCTCTTCCTGTCACCGACACTTCCTCAGCATCCACAGGTCAC
AA Mutation	p.His2973_Ala2974insThrThrProLeuProValThrAspThrSerSerAlaSerThrGlyHis(p.H2973_A2974insTTPLPVTDTSSASTGH)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

ID	32
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000463781
Start	195781035:195781036(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.10544_10545insAGGTGACACCACGACTCTTCCTGTCACCGACACTTCCTCAGTATCCACAGGTCACGCCACCCCTCTTCCTGTCACCAGCTTTTCCTCAGTATCCACAGGTGACACCACCCCTCTTCCTGTCACCGACGCTTCCTCGGCATCCAC
AA Mutation	p.Gly3516_His3517insAspThrThrThrLeuProValThrAspThrSerSerValSerThrGlyHisAlaThrProLeuProValThrSerPheSerSerValSerThrGlyAspThrThrProLeuProValThrAspAlaSerSerAlaSerThrGly(p.G3516_H3517insDTTTLPVTDTSSVSTGHATPLPVTSFSSVSTGDTTPLPVTDASSASTG)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

ID	33
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000463781
Start	195780994:195780995(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.10585_10586insCATCCACCGGTGACACCACGACTCTTCCTGTCACCGACACTTCCTCAGTATCCACAGGTCACGCCACCCCTCTTCCTGTCACCAGCTTTTCCTCAGTATCCACAGGTGACACCACCCCTCTTCCTGTCACCGACGCTTCCTCGGCATCCACCGGTCACGCTACCCCTCTTCCTGTCACCGACACTTCCTCAG
AA Mutation	p.Ser3528_Val3529insAlaSerThrGlyAspThrThrThrLeuProValThrAspThrSerSerValSerThrGlyHisAlaThrProLeuProValThrSerPheSerSerValSerThrGlyAspThrThrProLeuProValThrAspAlaSerSerAlaSerThrGlyHisAlaThrProLeuProValThrAspThrSerSer(p.S3528_V3529insASTGDTTTLPVTDTSSVSTGHATPLPVTSFSSVSTGDTTPLPVTDASSASTGHATPLPVTDTSS)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript