Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ADAMTS9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64622257:64622257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2627C>A
AA Mutation	p.Pro876His(p.P876H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64613469:64613469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3230T>C
AA Mutation	p.Val1077Ala(p.V1077A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64622446:64622446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759664813
CDS Mutation	c.2530C>T
AA Mutation	p.Arg844Cys(p.R844C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64596960:64596960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754078484
CDS Mutation	c.4049G>A
AA Mutation	p.Arg1350Gln(p.R1350Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000498707
Start	64654354:64654354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759029793
CDS Mutation	c.1315G>A
AA Mutation	p.Val439Met(p.V439M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64615991:64615991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201029802
CDS Mutation	c.2993C>T
AA Mutation	p.Thr998Met(p.T998M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64658570:64658570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.901G>A
AA Mutation	p.Ala301Thr(p.A301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64561737:64561737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4539T>G
AA Mutation	p.Cys1513Trp(p.C1513W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64633787:64633787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1949G>A
AA Mutation	p.Arg650Gln(p.R650Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64633791:64633791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1945T>G
AA Mutation	p.Phe649Val(p.F649V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64686633:64686633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451T>C
AA Mutation	p.Phe151Leu(p.F151L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64541118:64541118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5498A>T
AA Mutation	p.Asp1833Val(p.D1833V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64686800:64686800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284C>A
AA Mutation	p.Ser95Tyr(p.S95Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64533196:64533196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5688T>G
AA Mutation	p.Asn1896Lys(p.N1896K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64687564:64687564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94G>T
AA Mutation	p.Asp32Tyr(p.D32Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64621228:64621228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766944266
CDS Mutation	c.2699G>A
AA Mutation	p.Arg900Gln(p.R900Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64633809:64633809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1927C>A
AA Mutation	p.Leu643Ile(p.L643I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64551020:64551020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4741G>A
AA Mutation	p.Val1581Met(p.V1581M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64541590:64541590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5228A>G
AA Mutation	p.Lys1743Arg(p.K1743R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64622515:64622515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2461C>T
AA Mutation	p.Arg821Cys(p.R821C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64541188:64541188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577267039
CDS Mutation	c.5428C>T
AA Mutation	p.Arg1810Cys(p.R1810C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64594367:64594367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755716045
CDS Mutation	c.4247G>A
AA Mutation	p.Arg1416Gln(p.R1416Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64633830:64633830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1906T>C
AA Mutation	p.Ser636Pro(p.S636P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64686838:64686838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.246C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64681226:64681226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.654A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64613348:64613348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3351A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64654376:64654376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752019001
CDS Mutation	c.1293G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64522240:64522240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5739G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64621169:64621169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2758C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64621161:64621161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2766C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000498707
Start	64651020:64651020(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1460delT
AA Mutation	p.Leu487Ter(p.L487*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000498707
Start	64533233:64533233(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5651delC
AA Mutation	p.Ser1884PhefsTer2(p.S1884Ffs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000498707
Start	64604004:64604004(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3665delG
AA Mutation	p.Cys1222LeufsTer15(p.C1222Lfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000498707
Start	64561646:64561646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4630G>T
AA Mutation	p.Glu1544Ter(p.E1544*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000498707
Start	64633797:64633797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776836604
CDS Mutation	c.1939C>T
AA Mutation	p.Arg647Ter(p.R647*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000498707
Start	64621229:64621229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780201945
CDS Mutation	c.2698C>T
AA Mutation	p.Arg900Ter(p.R900*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000498707
Start	64613446:64613446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3253C>T
AA Mutation	p.Arg1085Ter(p.R1085*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ADAMTS9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64651041:64651041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779284125
CDS Mutation	c.1439G>A
AA Mutation	p.Arg480Gln(p.R480Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64541170:64541170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5446C>T
AA Mutation	p.Arg1816Trp(p.R1816W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64602138:64602138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371237082
CDS Mutation	c.3823C>T
AA Mutation	p.Arg1275Trp(p.R1275W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64551052:64551052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4709C>T
AA Mutation	p.Thr1570Ile(p.T1570I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000498707
Start	64533218:64533218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5666C>T
AA Mutation	p.Ala1889Val(p.A1889V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498707
Start	64631471:64631471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769078401
CDS Mutation	c.2373C>T
Mutation Classification	Silent
Feature Type	Transcript