Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MCF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139626288:139626288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592G>A
AA Mutation	p.Asp198Asn(p.D198N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139616288:139616288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1185G>T
AA Mutation	p.Glu395Asp(p.E395D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139629837:139629837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.296A>G
AA Mutation	p.Glu99Gly(p.E99G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139631424:139631424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.259T>G
AA Mutation	p.Cys87Gly(p.C87G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139616403:139616403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1070A>C
AA Mutation	p.Glu357Ala(p.E357A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139616309:139616309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1164T>G
AA Mutation	p.Phe388Leu(p.F388L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139597503:139597503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2012C>T
AA Mutation	p.Ser671Leu(p.S671L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139616403:139616403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1070A>G
AA Mutation	p.Glu357Gly(p.E357G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139615012:139615012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368001722
CDS Mutation	c.1232G>A
AA Mutation	p.Arg411Gln(p.R411Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139642500:139642500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186682047
CDS Mutation	c.19C>T
AA Mutation	p.Arg7Trp(p.R7W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139631469:139631469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>A
AA Mutation	p.Asp72Asn(p.D72N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139585157:139585157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2654C>A
AA Mutation	p.Ser885Tyr(p.S885Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139642472:139642472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.47A>G
AA Mutation	p.Asn16Ser(p.N16S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139626676:139626676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519T>G
AA Mutation	p.Ser173Arg(p.S173R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139588393:139588393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416A>C
AA Mutation	p.Asn806His(p.N806H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139585077:139585077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2734A>G
AA Mutation	p.Arg912Gly(p.R912G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139617569:139617569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943A>G
AA Mutation	p.Lys315Glu(p.K315E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139626726:139626726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469A>C
AA Mutation	p.Lys157Gln(p.K157Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139642487:139642487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.32T>C
AA Mutation	p.Met11Thr(p.M11T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370576
Start	139626700:139626700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.495G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370576
Start	139596699:139596699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2127T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370576
Start	139614893:139614893(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1351delT
AA Mutation	p.Ser451HisfsTer16(p.S451Hfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000370576
Start	139596570:139596570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2256C>G
AA Mutation	p.Tyr752Ter(p.Y752*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000370576
Start	139616413:139616413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1060C>T
AA Mutation	p.Gln354Ter(p.Q354*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000370576
Start	139619681:139619681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713T>A
AA Mutation	p.Leu238Ter(p.L238*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370576
Start	139619613:139619614(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.780dupA
AA Mutation	p.Leu261IlefsTer6(p.L261Ifs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370576
Start	139587779:139587780(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2458dupA
AA Mutation	p.Arg820LysfsTer12(p.R820Kfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MCF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139626694:139626694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501C>A
AA Mutation	p.Asp167Glu(p.D167E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139626660:139626660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535C>T
AA Mutation	p.His179Tyr(p.H179Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139596636:139596636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2190A>C
AA Mutation	p.Glu730Asp(p.E730D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370576
Start	139615012:139615012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368001722
CDS Mutation	c.1232G>A
AA Mutation	p.Arg411Gln(p.R411Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000370576
Start	139588402:139588402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2407G>T
AA Mutation	p.Glu803Ter(p.E803*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000370576
Start	139607780:139607780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1402-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript