Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ADAMTS5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26966027:26966027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365C>G
AA Mutation	p.Ala122Gly(p.A122G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26924406:26924406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2440A>G
AA Mutation	p.Arg814Gly(p.R814G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26965829:26965829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371256284
CDS Mutation	c.563G>A
AA Mutation	p.Arg188Gln(p.R188Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26965911:26965911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145627700
CDS Mutation	c.481G>A
AA Mutation	p.Ala161Thr(p.A161T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26932056:26932056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1997A>T
AA Mutation	p.Lys666Met(p.K666M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26966109:26966109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.283G>A
AA Mutation	p.Gly95Ser(p.G95S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26932144:26932144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1909A>G
AA Mutation	p.Asn637Asp(p.N637D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26934525:26934525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1630A>G
AA Mutation	p.Lys544Glu(p.K544E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26943517:26943517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1268C>T
AA Mutation	p.Ser423Phe(p.S423F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26924540:26924540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2306C>T
AA Mutation	p.Thr769Ile(p.T769I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26965881:26965881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511G>A
AA Mutation	p.Gly171Arg(p.G171R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26924216:26924216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750142658
CDS Mutation	c.2630C>T
AA Mutation	p.Pro877Leu(p.P877L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26930048:26930048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2063C>G
AA Mutation	p.Thr688Ser(p.T688S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26954765:26954765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1211C>T
AA Mutation	p.Ala404Val(p.A404V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26965970:26965970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751039845
CDS Mutation	c.422G>A
AA Mutation	p.Arg141His(p.R141H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26966115:26966115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277G>A
AA Mutation	p.Ala93Thr(p.A93T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26932089:26932089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1964A>G
AA Mutation	p.Lys655Arg(p.K655R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26934665:26934665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759694630
CDS Mutation	c.1490G>A
AA Mutation	p.Cys497Tyr(p.C497Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26943475:26943475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367992476
CDS Mutation	c.1310G>A
AA Mutation	p.Arg437His(p.R437H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26965665:26965665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727G>A
AA Mutation	p.Ala243Thr(p.A243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26934672:26934672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483C>A
AA Mutation	p.Gln495Lys(p.Q495K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26934547:26934547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149804004
CDS Mutation	c.1608G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26930017:26930017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372646537
CDS Mutation	c.2094C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26965924:26965924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781071406
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26966119:26966119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.273C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26965852:26965852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26966026:26966026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375872938
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26934685:26934685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1470C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26965882:26965882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26965981:26965981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751691727
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26966107:26966107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26966035:26966035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26954767:26954767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774940785
CDS Mutation	c.1209C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26965909:26965909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000284987
Start	26965290:26965290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102G>T
AA Mutation	p.Glu368Ter(p.E368*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000284987
Start	26934507:26934507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648C>T
AA Mutation	p.Gln550Ter(p.Q550*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284987
Start	26934474:26934475(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1680dupA
AA Mutation	p.Tyr561IlefsTer35(p.Y561Ifs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ADAMTS5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26966121:26966121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>A
AA Mutation	p.Val91Ile(p.V91I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26966134:26966134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258G>T
AA Mutation	p.Lys86Asn(p.K86N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284987
Start	26924298:26924298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2548T>G
AA Mutation	p.Phe850Val(p.F850V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26965819:26965819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284987
Start	26943417:26943417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1368T>G
Mutation Classification	Silent
Feature Type	Transcript