Colon Cancer: Gene >> KAT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219797
Start	31130786:31130786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1198C>A
AA Mutation	p.Leu400Met(p.L400M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219797
Start	31130060:31130060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.815A>T
AA Mutation	p.Asp272Val(p.D272V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219797
Start	31130820:31130820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1232G>A
AA Mutation	p.Gly411Asp(p.G411D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219797
Start	31127059:31127059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747070698
CDS Mutation	c.487A>G
AA Mutation	p.Thr163Ala(p.T163A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219797
Start	31120502:31120502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219797
Start	31117831:31117831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219797
Start	31120377:31120377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219797
Start	31130058:31130058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000219797
Start	31130315:31130315(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.966delC
AA Mutation	p.Tyr323ThrfsTer48(p.Y323Tfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000219797
Start	31128070:31128071(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs773168027
CDS Mutation	c.708dupC
AA Mutation	p.Gly237ArgfsTer16(p.G237Rfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KAT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219797
Start	31120344:31120344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>T
AA Mutation	p.Arg98Trp(p.R98W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript