Colon Cancer: Gene >> NADK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341426
Start	1765395:1765395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12A>C
AA Mutation	p.Glu4Asp(p.E4D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341426
Start	1752957:1752957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1288C>T
AA Mutation	p.Arg430Trp(p.R430W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341426
Start	1754608:1754608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779G>A
AA Mutation	p.Gly260Asp(p.G260D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341426
Start	1754115:1754115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037C>T
AA Mutation	p.Thr346Met(p.T346M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341426
Start	1765325:1765325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373135938
CDS Mutation	c.82G>A
AA Mutation	p.Gly28Ser(p.G28S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341426
Start	1754169:1754169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983C>T
AA Mutation	p.Ala328Val(p.A328V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341426
Start	1754643:1754643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341426
Start	1754162:1754162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558595198
CDS Mutation	c.990G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341426
Start	1761962:1761962(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.253delC
AA Mutation	p.Gln85ArgfsTer14(p.Q85Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341426
Start	1756295:1756295(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.548delG
AA Mutation	p.Gly183GlufsTer30(p.G183Efs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NADK

No Mutation Annotation!