Colon Cancer: Gene >> PRKAB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229328
Start	119668365:119668365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772422545
CDS Mutation	c.121C>T
AA Mutation	p.Pro41Ser(p.P41S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229328
Start	119679988:119679988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568377821
CDS Mutation	c.722C>T
AA Mutation	p.Ala241Val(p.A241V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229328
Start	119672355:119672355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214A>G
AA Mutation	p.Lys72Glu(p.K72E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229328
Start	119679943:119679943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677C>A
AA Mutation	p.Ala226Asp(p.A226D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229328
Start	119672401:119672401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260G>A
AA Mutation	p.Gly87Asp(p.G87D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229328
Start	119672366:119672366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRKAB1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000229328
Start	119674057:119674057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417G>T
AA Mutation	p.Glu139Asp(p.E139D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229328
Start	119674445:119674445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762004648
CDS Mutation	c.523G>A
AA Mutation	p.Asp175Asn(p.D175N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript