Colon Cancer: Gene >> GCKR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264717
Start	27505743:27505743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146168012
CDS Mutation	c.776G>A
AA Mutation	p.Arg259Gln(p.R259Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264717
Start	27523281:27523281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761397252
CDS Mutation	c.1720G>A
AA Mutation	p.Ala574Thr(p.A574T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264717
Start	27503617:27503617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374489109
CDS Mutation	c.748G>A
AA Mutation	p.Gly250Arg(p.G250R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264717
Start	27507982:27507982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246C>T
AA Mutation	p.Leu416Phe(p.L416F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264717
Start	27503563:27503563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763108416
CDS Mutation	c.694C>T
AA Mutation	p.Arg232Trp(p.R232W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264717
Start	27522468:27522468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144661986
CDS Mutation	c.1581T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264717
Start	27503616:27503616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371788464
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264717
Start	27508185:27508185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1356C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264717
Start	27522477:27522477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1590C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GCKR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264717
Start	27507241:27507241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1073G>T
AA Mutation	p.Arg358Leu(p.R358L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264717
Start	27496917:27496917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13A>G
AA Mutation	p.Lys5Glu(p.K5E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript