Colon Cancer: Gene >> EAF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273668
Start	121872562:121872562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>T
AA Mutation	p.Met170Ile(p.M170I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273668
Start	121854781:121854781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774441301
CDS Mutation	c.296G>A
AA Mutation	p.Arg99Gln(p.R99Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273668
Start	121854732:121854732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247T>G
AA Mutation	p.Tyr83Asp(p.Y83D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273668
Start	121857149:121857149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746294937
CDS Mutation	c.477C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273668
Start	121854721:121854722(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.243dupA
AA Mutation	p.Pro82ThrfsTer11(p.P82Tfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EAF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273668
Start	121854780:121854780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377108596
CDS Mutation	c.295C>T
AA Mutation	p.Arg99Trp(p.R99W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript