Colon Cancer: Gene >> HNRNPK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351839
Start	83972069:83972069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766C>T
AA Mutation	p.Arg256Trp(p.R256W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000351839
Start	83977690:83977690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.155A>T
AA Mutation	p.Lys52Met(p.K52M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000351839
Start	83971716:83971716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964G>A
AA Mutation	p.Ala322Thr(p.A322T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000351839
Start	83970283:83970283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1240C>T
AA Mutation	p.Arg414Cys(p.R414C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000351839
Start	83972095:83972095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.740G>A
AA Mutation	p.Arg247His(p.R247H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000351839
Start	83972144:83972144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691G>A
AA Mutation	p.Asp231Asn(p.D231N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351839
Start	83971902:83971902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000351839
Start	83970896:83970896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1108+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000351839
Start	83973285:83973285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351839
Start	83971298:83971298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1067A>C
AA Mutation	p.Glu356Ala(p.E356A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000351839
Start	83973928:83973928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376G>A
AA Mutation	p.Glu126Lys(p.E126K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript