Colon Cancer: Gene >> AK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373156
Start	127871917:127871917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375921903
CDS Mutation	c.230G>A
AA Mutation	p.Arg77Gln(p.R77Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373156
Start	127868359:127868359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201971818
CDS Mutation	c.478G>A
AA Mutation	p.Val160Ile(p.V160I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373156
Start	127872812:127872812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150701679
CDS Mutation	c.85G>A
AA Mutation	p.Val29Met(p.V29M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373156
Start	127871824:127871824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323G>T
AA Mutation	p.Arg108Leu(p.R108L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373156
Start	127868480:127868480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373156
Start	127868416:127868416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761271981
CDS Mutation	c.421G>A
AA Mutation	p.Asp141Asn(p.D141N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript