Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> STK31

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23781477:23781477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758070947
CDS Mutation	c.2024G>A
AA Mutation	p.Arg675His(p.R675H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23729165:23729165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.399G>T
AA Mutation	p.Glu133Asp(p.E133D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23790831:23790831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2645G>A
AA Mutation	p.Arg882Gln(p.R882Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23769070:23769070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1492T>A
AA Mutation	p.Phe498Ile(p.F498I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23769682:23769682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1639G>A
AA Mutation	p.Ala547Thr(p.A547T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23786916:23786916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2479A>C
AA Mutation	p.Asn827His(p.N827H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23832262:23832262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2956G>T
AA Mutation	p.Asp986Tyr(p.D986Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23815148:23815148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2765C>A
AA Mutation	p.Ser922Tyr(p.S922Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23790930:23790930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2744G>A
AA Mutation	p.Gly915Asp(p.G915D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23754417:23754417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1236G>T
AA Mutation	p.Glu412Asp(p.E412D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23762912:23762912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1405A>C
AA Mutation	p.Lys469Gln(p.K469Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23769102:23769102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1524G>C
AA Mutation	p.Glu508Asp(p.E508D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23790917:23790917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2731T>G
AA Mutation	p.Leu911Val(p.L911V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355870
Start	23729247:23729247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481C>G
AA Mutation	p.Gln161Glu(p.Q161E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23729221:23729221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.455C>A
AA Mutation	p.Ser152Tyr(p.S152Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23790905:23790905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2719C>T
AA Mutation	p.Pro907Ser(p.P907S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23735843:23735843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.789G>T
AA Mutation	p.Met263Ile(p.M263I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23712254:23712254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118C>G
AA Mutation	p.His40Asp(p.H40D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23729109:23729109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343G>T
AA Mutation	p.Asp115Tyr(p.D115Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23712137:23712137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.89A>G
AA Mutation	p.Tyr30Cys(p.Y30C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23762906:23762906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199698256
CDS Mutation	c.1399C>T
AA Mutation	p.Arg467Cys(p.R467C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23735595:23735595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.541G>A
AA Mutation	p.Ala181Thr(p.A181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355870
Start	23790898:23790898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2712T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355870
Start	23762911:23762911(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1408delA
AA Mutation	p.Thr470HisfsTer9(p.T470Hfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355870
Start	23735722:23735722(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746386632
CDS Mutation	c.675delA
AA Mutation	p.Lys225AsnfsTer35(p.K225Nfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355870
Start	23832252:23832252(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2948delC
AA Mutation	p.Pro983GlnfsTer16(p.P983Qfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000355870
Start	23736986:23736986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925G>T
AA Mutation	p.Glu309Ter(p.E309*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000355870
Start	23752825:23752825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1126G>T
AA Mutation	p.Glu376Ter(p.E376*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000355870
Start	23786850:23786851(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2413_2414insGATAATTTTT
AA Mutation	p.Ala805GlyfsTer2(p.A805Gfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000355870
Start	23769064:23769064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1486A>T
AA Mutation	p.Lys496Ter(p.K496*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355870
Start	23790896:23790897(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2710_2711insAATATTTTACATATTT
AA Mutation	p.Pro904GlnfsTer31(p.P904Qfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000355870
Start	23815143:23815143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2761-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000355870
Start	23727316:23727316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.324+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000355870
Start	23752816:23752817(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1117_1118insCTG
AA Mutation	p.Ile373delinsThrVal(p.I373delinsTV)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000355870
Start	23752818:23752819(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1119_1120insTTT
AA Mutation	p.Ile373_Leu374insPhe(p.I373_L374insF)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> STK31

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23832179:23832179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2873G>C
AA Mutation	p.Arg958Thr(p.R958T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23772273:23772273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1960G>A
AA Mutation	p.Glu654Lys(p.E654K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23736957:23736957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896A>C
AA Mutation	p.Lys299Thr(p.K299T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355870
Start	23754322:23754322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757104552
CDS Mutation	c.1141G>A
AA Mutation	p.Asp381Asn(p.D381N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355870
Start	23717504:23717504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355870
Start	23762908:23762908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1401C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355870
Start	23769732:23769732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1689C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355870
Start	23712271:23712271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135A>C
Mutation Classification	Silent
Feature Type	Transcript