Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DOCK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127000229:127000229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907C>T
AA Mutation	p.Arg303Cys(p.R303C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000280333
Start	127410923:127410923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200693040
CDS Mutation	c.4364C>T
AA Mutation	p.Ala1455Val(p.A1455V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127418411:127418411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557337834
CDS Mutation	c.4499C>T
AA Mutation	p.Thr1500Met(p.T1500M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127018793:127018793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372560858
CDS Mutation	c.1222G>A
AA Mutation	p.Ala408Thr(p.A408T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	126998098:126998098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616A>C
AA Mutation	p.Lys206Gln(p.K206Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127110321:127110321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2527G>A
AA Mutation	p.Glu843Lys(p.E843K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127433319:127433319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4888C>G
AA Mutation	p.Arg1630Gly(p.R1630G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127409118:127409118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778556643
CDS Mutation	c.4141G>A
AA Mutation	p.Ala1381Thr(p.A1381T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127052794:127052794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2252G>A
AA Mutation	p.Arg751His(p.R751H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127418536:127418536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4624G>A
AA Mutation	p.Glu1542Lys(p.E1542K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127419741:127419741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4705G>T
AA Mutation	p.Ala1569Ser(p.A1569S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127409387:127409387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4276G>C
AA Mutation	p.Val1426Leu(p.V1426L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127384893:127384893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3848A>G
AA Mutation	p.Tyr1283Cys(p.Y1283C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127248030:127248030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2807C>T
AA Mutation	p.Thr936Ile(p.T936I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127384890:127384890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3845A>G
AA Mutation	p.His1282Arg(p.H1282R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127384811:127384811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3766G>A
AA Mutation	p.Ala1256Thr(p.A1256T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127447469:127447469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5426C>T
AA Mutation	p.Ala1809Val(p.A1809V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127439095:127439095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5066A>G
AA Mutation	p.Asp1689Gly(p.D1689G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127024741:127024741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1446T>G
AA Mutation	p.Ile482Met(p.I482M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	126996788:126996788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514A>T
AA Mutation	p.Asn172Tyr(p.N172Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127409077:127409077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750915688
CDS Mutation	c.4100G>A
AA Mutation	p.Arg1367Gln(p.R1367Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127362200:127362200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3357A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127447512:127447512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5469G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127037732:127037732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1863G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127418493:127418493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185222787
CDS Mutation	c.4581C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127404414:127404414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127409120:127409120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771141839
CDS Mutation	c.4143C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127447464:127447464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755126443
CDS Mutation	c.5421C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127409117:127409117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768238882
CDS Mutation	c.4140C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	126987542:126987542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201302163
CDS Mutation	c.249G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127032169:127032169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368325806
CDS Mutation	c.1698G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000280333
Start	127023208:127023208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273C>T
AA Mutation	p.Arg425Ter(p.R425*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DOCK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127410916:127410916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777850348
CDS Mutation	c.4357G>C
AA Mutation	p.Glu1453Gln(p.E1453Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127127720:127127720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2740G>T
AA Mutation	p.Val914Leu(p.V914L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127037739:127037739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1870A>G
AA Mutation	p.Lys624Glu(p.K624E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280333
Start	127110321:127110321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2527G>A
AA Mutation	p.Glu843Lys(p.E843K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127374160:127374160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3558C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127257415:127257415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2967C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127042705:127042705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2028T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127026378:127026378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774326772
CDS Mutation	c.1515C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280333
Start	127444182:127444182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143736792
CDS Mutation	c.5253C>T
Mutation Classification	Silent
Feature Type	Transcript