Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NCOA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34727400:34727400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6007C>T
AA Mutation	p.Pro2003Ser(p.P2003S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34740989:34740989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5267C>A
AA Mutation	p.Ser1756Tyr(p.S1756Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34742630:34742630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3626C>T
AA Mutation	p.Pro1209Leu(p.P1209L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34732577:34732577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369844271
CDS Mutation	c.5981C>T
AA Mutation	p.Ala1994Val(p.A1994V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34754857:34754857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532522078
CDS Mutation	c.1540C>T
AA Mutation	p.Arg514Cys(p.R514C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34758002:34758002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.746A>G
AA Mutation	p.Asn249Ser(p.N249S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34741814:34741814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4442C>A
AA Mutation	p.Ser1481Tyr(p.S1481Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34741130:34741130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5126C>A
AA Mutation	p.Ser1709Tyr(p.S1709Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34776401:34776401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368096873
CDS Mutation	c.283C>T
AA Mutation	p.Arg95Cys(p.R95C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34757697:34757697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751187935
CDS Mutation	c.1051G>A
AA Mutation	p.Gly351Ser(p.G351S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34757432:34757432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1316C>T
AA Mutation	p.Ser439Phe(p.S439F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34750094:34750094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2101C>G
AA Mutation	p.Pro701Ala(p.P701A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34740663:34740663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5593A>G
AA Mutation	p.Met1865Val(p.M1865V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34742705:34742705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3551C>T
AA Mutation	p.Pro1184Leu(p.P1184L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34742516:34742516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3740C>T
AA Mutation	p.Ser1247Phe(p.S1247F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34754818:34754818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579A>C
AA Mutation	p.Asn527His(p.N527H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34742840:34742840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3416A>G
AA Mutation	p.Glu1139Gly(p.E1139G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34727351:34727351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6056G>A
AA Mutation	p.Arg2019Gln(p.R2019Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34742964:34742964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3292C>T
AA Mutation	p.Pro1098Ser(p.P1098S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359003
Start	34757938:34757938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359003
Start	34768522:34768522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359003
Start	34741861:34741861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201911903
CDS Mutation	c.4395G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359003
Start	34749702:34749702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2493T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359003
Start	34757395:34757395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359003
Start	34750230:34750230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1965T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359003
Start	34749465:34749465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372333834
CDS Mutation	c.2730C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359003
Start	34742650:34742650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372455229
CDS Mutation	c.3606G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359003
Start	34750086:34750086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2109G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359003
Start	34742743:34742743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747102209
CDS Mutation	c.3513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359003
Start	34750026:34750026(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2169delG
AA Mutation	p.Asn724IlefsTer20(p.N724Ifs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359003
Start	34750198:34750198(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1997delC
AA Mutation	p.Pro666ArgfsTer12(p.P666Rfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000359003
Start	34740963:34740963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5293G>T
AA Mutation	p.Glu1765Ter(p.E1765*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359003
Start	34742754:34742755(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3501dupA
AA Mutation	p.Pro1168ThrfsTer41(p.P1168Tfs*41)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NCOA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34776297:34776297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387T>G
AA Mutation	p.Ile129Met(p.I129M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34741677:34741677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4579A>G
AA Mutation	p.Lys1527Glu(p.K1527E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34740750:34740750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5506A>G
AA Mutation	p.Thr1836Ala(p.T1836A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34741130:34741130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5126C>A
AA Mutation	p.Ser1709Tyr(p.S1709Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34742336:34742336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3920C>A
AA Mutation	p.Ser1307Tyr(p.S1307Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359003
Start	34742899:34742899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3357G>T
AA Mutation	p.Gln1119His(p.Q1119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359003
Start	34740997:34740997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5259T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000359003
Start	34741632:34741632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4624G>T
AA Mutation	p.Glu1542Ter(p.E1542*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript