Colon Cancer: Gene >> IFNA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380206
Start	21384812:21384812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772553727
CDS Mutation	c.518C>G
AA Mutation	p.Ser173Cys(p.S173C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380206
Start	21385193:21385193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137G>T
AA Mutation	p.Arg46Ile(p.R46I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380206
Start	21384903:21384903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373475123
CDS Mutation	c.427A>G
AA Mutation	p.Arg143Gly(p.R143G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380206
Start	21385051:21385051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279G>T
AA Mutation	p.Lys93Asn(p.K93N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380206
Start	21384876:21384876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454T>C
AA Mutation	p.Tyr152His(p.Y152H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IFNA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380206
Start	21384887:21384887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443G>T
AA Mutation	p.Arg148Ile(p.R148I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript