Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KLHL20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000209884
Start	173785188:173785188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1771C>T
AA Mutation	p.Arg591Trp(p.R591W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000209884
Start	173756986:173756986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.978G>C
AA Mutation	p.Trp326Cys(p.W326C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000209884
Start	173774355:173774355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346G>A
AA Mutation	p.Arg449Lys(p.R449K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000209884
Start	173734147:173734147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.458T>C
AA Mutation	p.Ile153Thr(p.I153T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000209884
Start	173733814:173733814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125G>A
AA Mutation	p.Arg42His(p.R42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000209884
Start	173756003:173756003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932G>A
AA Mutation	p.Arg311Gln(p.R311Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000209884
Start	173782201:173782201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1716A>C
AA Mutation	p.Glu572Asp(p.E572D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000209884
Start	173757021:173757021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013A>G
AA Mutation	p.Tyr338Cys(p.Y338C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000209884
Start	173785188:173785188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1771C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000209884
Start	173757124:173757124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000209884
Start	173775830:173775830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1626A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000209884
Start	173766194:173766194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1200C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000209884
Start	173716067:173716067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.23+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KLHL20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000209884
Start	173751846:173751846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680G>A
AA Mutation	p.Ser227Asn(p.S227N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000209884
Start	173753271:173753271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815G>T
AA Mutation	p.Gly272Val(p.G272V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000209884
Start	173716063:173716063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.20G>A
AA Mutation	p.Arg7His(p.R7H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript