Colon Cancer: Gene >> HK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359426
Start	69384865:69384865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1789C>T
AA Mutation	p.Pro597Ser(p.P597S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359426
Start	69377025:69377025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770084986
CDS Mutation	c.967C>T
AA Mutation	p.Arg323Trp(p.R323W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359426
Start	69395056:69395056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1054203
CDS Mutation	c.2326C>A
AA Mutation	p.Leu776Met(p.L776M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359426
Start	69401110:69401110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775763125
CDS Mutation	c.2729G>A
AA Mutation	p.Arg910Gln(p.R910Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359426
Start	69380023:69380023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775082107
CDS Mutation	c.1193G>A
AA Mutation	p.Arg398His(p.R398H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359426
Start	69382695:69382695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373626952
CDS Mutation	c.1474C>T
AA Mutation	p.Arg492Trp(p.R492W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359426
Start	69384839:69384839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1763A>T
AA Mutation	p.Tyr588Phe(p.Y588F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359426
Start	69392274:69392274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2185G>T
AA Mutation	p.Val729Leu(p.V729L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359426
Start	69380004:69380004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140290094
CDS Mutation	c.1174G>A
AA Mutation	p.Ala392Thr(p.A392T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359426
Start	69394993:69394993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762936110
CDS Mutation	c.2263C>T
AA Mutation	p.Arg755Cys(p.R755C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359426
Start	69369586:69369586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359426
Start	69398676:69398676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2457C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359426
Start	69360024:69360024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533615871
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359426
Start	69359913:69359913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000359426
Start	69379890:69379890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1060G>T
AA Mutation	p.Glu354Ter(p.E354*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359426
Start	69394997:69394997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2267A>C
AA Mutation	p.Asn756Thr(p.N756T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359426
Start	69364845:69364845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438G>A
Mutation Classification	Silent
Feature Type	Transcript