Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZDHHC21

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000380916
Start	14619641:14619641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663T>G
AA Mutation	p.Asp221Glu(p.D221E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380916
Start	14658879:14658879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775081820
CDS Mutation	c.374A>G
AA Mutation	p.Asn125Ser(p.N125S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380916
Start	14674271:14674271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70T>A
AA Mutation	p.Trp24Arg(p.W24R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380916
Start	14639926:14639926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380916
Start	14619088:14619088(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.676delC
AA Mutation	p.Arg226GlufsTer61(p.R226Efs*61)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZDHHC21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380916
Start	14674313:14674313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28G>T
AA Mutation	p.Asp10Tyr(p.D10Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380916
Start	14619087:14619087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61752940
CDS Mutation	c.677G>A
AA Mutation	p.Arg226Gln(p.R226Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380916
Start	14662299:14662299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281A>C
AA Mutation	p.Lys94Thr(p.K94T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000380916
Start	14672829:14672829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript