Colon Cancer: Gene >> HK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74889450:74889450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2581G>T
AA Mutation	p.Asp861Tyr(p.D861Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74880383:74880383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1384C>T
AA Mutation	p.Arg462Trp(p.R462W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74889312:74889312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2443G>A
AA Mutation	p.Asp815Asn(p.D815N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74886532:74886532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2078T>C
AA Mutation	p.Val693Ala(p.V693A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74854317:74854317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567201785
CDS Mutation	c.88C>T
AA Mutation	p.Arg30Cys(p.R30C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74877228:74877228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.938T>C
AA Mutation	p.Met313Thr(p.M313T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74881771:74881771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs62642507
CDS Mutation	c.1631G>A
AA Mutation	p.Arg544His(p.R544H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74886526:74886526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746400081
CDS Mutation	c.2072G>A
AA Mutation	p.Arg691His(p.R691H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74880293:74880293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148796379
CDS Mutation	c.1294C>T
AA Mutation	p.Arg432Trp(p.R432W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74881805:74881805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1665G>A
AA Mutation	p.Met555Ile(p.M555I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74890891:74890891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2704G>A
AA Mutation	p.Ala902Thr(p.A902T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290573
Start	74878871:74878871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779743587
CDS Mutation	c.1215G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290573
Start	74874309:74874309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373457354
CDS Mutation	c.735C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290573
Start	74881739:74881739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1599T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290573
Start	74873326:74873326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.546C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290573
Start	74881820:74881820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369669565
CDS Mutation	c.1680C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000290573
Start	74881743:74881743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1603G>T
AA Mutation	p.Gly535Ter(p.G535*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000290573
Start	74881803:74881804(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1663_1664insCAG
AA Mutation	p.Met555delinsThrVal(p.M555delinsTV)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74886524:74886524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2070G>A
AA Mutation	p.Met690Ile(p.M690I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290573
Start	74880503:74880503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199889864
CDS Mutation	c.1504G>A
AA Mutation	p.Glu502Lys(p.E502K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript