Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KCNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49373848:49373848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1712C>T
AA Mutation	p.Pro571Leu(p.P571L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374866:49374866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694G>A
AA Mutation	p.Val232Met(p.V232M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374682:49374682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878G>A
AA Mutation	p.Arg293His(p.R293H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374265:49374265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1295G>A
AA Mutation	p.Arg432Gln(p.R432Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49373099:49373099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2461A>T
AA Mutation	p.Thr821Ser(p.T821S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49482426:49482426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.55G>A
AA Mutation	p.Glu19Lys(p.E19K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49373444:49373444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779750227
CDS Mutation	c.2116G>A
AA Mutation	p.Ala706Thr(p.A706T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49373951:49373951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1609G>A
AA Mutation	p.Ala537Thr(p.A537T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49482287:49482287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.194C>T
AA Mutation	p.Thr65Met(p.T65M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374586:49374586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759765009
CDS Mutation	c.974G>A
AA Mutation	p.Arg325Gln(p.R325Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374542:49374542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1018A>G
AA Mutation	p.Met340Val(p.M340V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49482314:49482314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167G>A
AA Mutation	p.Arg56Gln(p.R56Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374091:49374091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1469G>T
AA Mutation	p.Trp490Leu(p.W490L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374236:49374236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1324A>G
AA Mutation	p.Asn442Asp(p.N442D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374652:49374652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.908G>A
AA Mutation	p.Arg303Gln(p.R303Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49373470:49373470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2090A>G
AA Mutation	p.Asn697Ser(p.N697S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49373962:49373962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1598A>G
AA Mutation	p.Tyr533Cys(p.Y533C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374680:49374680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880C>T
AA Mutation	p.Arg294Cys(p.R294C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49482282:49482282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>A
AA Mutation	p.Asp67Asn(p.D67N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49373692:49373692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1868A>G
AA Mutation	p.Glu623Gly(p.E623G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49482320:49482320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161G>A
AA Mutation	p.Arg54His(p.R54H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49482183:49482183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Cys(p.R100C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49374687:49374687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.873T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49373739:49373739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1821C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49481977:49481977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139960830
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49373133:49373133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2427A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49374303:49374303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49482009:49482009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000371741
Start	49373155:49373155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2405T>G
AA Mutation	p.Leu802Ter(p.L802*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000371741
Start	49373075:49373075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2485G>T
AA Mutation	p.Glu829Ter(p.E829*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371741
Start	49373234:49373235(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs747521886
CDS Mutation	c.2325dupC
AA Mutation	p.Lys776GlnfsTer23(p.K776Qfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371741
Start	49374356:49374357(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1196_1203dupTTGCAGGA
AA Mutation	p.Val402LeufsTer6(p.V402Lfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KCNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49482182:49482182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299G>A
AA Mutation	p.Arg100His(p.R100H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49373604:49373604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1956C>A
AA Mutation	p.Phe652Leu(p.F652L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371741
Start	49374272:49374272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1288A>C
AA Mutation	p.Ile430Leu(p.I430L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49482211:49482211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762279881
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49374900:49374900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751017425
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49374798:49374798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.762G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371741
Start	49373145:49373145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2415C>T
Mutation Classification	Silent
Feature Type	Transcript