Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAP3K4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161084572:161084572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2327A>G
AA Mutation	p.Glu776Gly(p.E776G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161073593:161073593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2078A>T
AA Mutation	p.Asp693Val(p.D693V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161048955:161048955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683C>G
AA Mutation	p.Thr228Ser(p.T228S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161098301:161098301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3548C>T
AA Mutation	p.Ala1183Val(p.A1183V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049056:161049056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>A
AA Mutation	p.Glu262Lys(p.E262K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161102748:161102748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3825G>T
AA Mutation	p.Trp1275Cys(p.W1275C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161111953:161111953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4514C>T
AA Mutation	p.Thr1505Ile(p.T1505I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161107946:161107946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4096G>A
AA Mutation	p.Gly1366Arg(p.G1366R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049719:161049719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1447G>A
AA Mutation	p.Asp483Asn(p.D483N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049096:161049096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747759728
CDS Mutation	c.824G>A
AA Mutation	p.Arg275Gln(p.R275Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161111839:161111839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4400C>T
AA Mutation	p.Ala1467Val(p.A1467V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161048689:161048689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417C>A
AA Mutation	p.Ser139Arg(p.S139R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161107961:161107961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4111A>G
AA Mutation	p.Met1371Val(p.M1371V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161098354:161098354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3601G>A
AA Mutation	p.Ala1201Thr(p.A1201T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161112695:161112695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773556218
CDS Mutation	c.4547G>A
AA Mutation	p.Arg1516His(p.R1516H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049287:161049287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1015A>T
AA Mutation	p.Thr339Ser(p.T339S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049743:161049743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1471T>G
AA Mutation	p.Ser491Ala(p.S491A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161093021:161093021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3313G>A
AA Mutation	p.Ala1105Thr(p.A1105T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161034340:161034340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.234G>T
AA Mutation	p.Glu78Asp(p.E78D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161048961:161048961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771620324
CDS Mutation	c.689G>A
AA Mutation	p.Arg230Gln(p.R230Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392142
Start	161049730:161049730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566150221
CDS Mutation	c.1458G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392142
Start	161109842:161109842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4324C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392142
Start	160992024:160992024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.93G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392142
Start	161034272:161034272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200166879
CDS Mutation	c.166T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392142
Start	161048659:161048659(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.391delA
AA Mutation	p.Thr131GlnfsTer37(p.T131Qfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392142
Start	161084537:161084537(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2297delT
AA Mutation	p.Leu766Ter(p.L766*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392142
Start	161048797:161048797(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.531delA
AA Mutation	p.Lys177AsnfsTer30(p.K177Nfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392142
Start	161048744:161048744(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.479delA
AA Mutation	p.Asn160MetfsTer8(p.N160Mfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000392142
Start	161115177:161115177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4681G>T
AA Mutation	p.Gly1561Ter(p.G1561*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000392142
Start	161081019:161081019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2236C>T
AA Mutation	p.Gln746Ter(p.Q746*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000392142
Start	161091502:161091502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3097C>T
AA Mutation	p.Arg1033Ter(p.R1033*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000392142
Start	161048686:161048686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.414C>A
AA Mutation	p.Tyr138Ter(p.Y138*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392142
Start	161048743:161048744(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.479dupA
AA Mutation	p.Asn160LysfsTer27(p.N160Kfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392142
Start	161048796:161048797(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.531dupA
AA Mutation	p.Ser178IlefsTer9(p.S178Ifs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAP3K4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161101918:161101918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3701G>A
AA Mutation	p.Arg1234Gln(p.R1234Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161048936:161048936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Cys(p.R222C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392142
Start	161049279:161049279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007G>A
AA Mutation	p.Gly336Asp(p.G336D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392142
Start	161089441:161089441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368962247
CDS Mutation	c.2943G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392142
Start	161048986:161048986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000392142
Start	161034374:161034374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370191115
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Ter(p.R90*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000392142
Start	161106561:161106561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3904C>T
AA Mutation	p.Arg1302Ter(p.R1302*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript