Colon Cancer: Gene >> NKX2-3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344586
Start	99535272:99535272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646G>A
AA Mutation	p.Ala216Thr(p.A216T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344586
Start	99533220:99533220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89C>T
AA Mutation	p.Ala30Val(p.A30V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344586
Start	99533437:99533437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306C>A
AA Mutation	p.Ser102Arg(p.S102R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344586
Start	99533437:99533437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NKX2-3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344586
Start	99533160:99533160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29C>T
AA Mutation	p.Thr10Ile(p.T10I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript