Colon Cancer: Gene >> GCK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000403799
Start	44145576:44145576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1174C>T
AA Mutation	p.Arg392Cys(p.R392C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000403799
Start	44149976:44149976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572G>A
AA Mutation	p.Arg191Gln(p.R191Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000403799
Start	44152333:44152333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762922697
CDS Mutation	c.301G>A
AA Mutation	p.Val101Met(p.V101M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000403799
Start	44145716:44145716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034G>A
AA Mutation	p.Arg345His(p.R345H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000403799
Start	44145270:44145270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1264C>T
AA Mutation	p.Arg422Trp(p.R422W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403799
Start	44147679:44147679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200071687
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403799
Start	44150005:44150005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777964292
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403799
Start	44149779:44149779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142952813
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403799
Start	44150014:44150014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749386678
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403799
Start	44147721:44147721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754094813
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403799
Start	44149773:44149773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193922318
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403799
Start	44145529:44145529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000403799
Start	44145281:44145281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GCK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000403799
Start	44145251:44145251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1283G>A
AA Mutation	p.Arg428His(p.R428H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000403799
Start	44145555:44145555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757888672
CDS Mutation	c.1195G>A
AA Mutation	p.Glu399Lys(p.E399K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403799
Start	44145196:44145196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1338C>T
Mutation Classification	Silent
Feature Type	Transcript