Colon Cancer: Gene >> NKX6-2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368592
Start	132785047:132785047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703G>A
AA Mutation	p.Asp235Asn(p.D235N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368592
Start	132785136:132785136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614A>T
AA Mutation	p.Lys205Met(p.K205M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368592
Start	132785056:132785056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.694G>A
AA Mutation	p.Ala232Thr(p.A232T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368592
Start	132785423:132785423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758939375
CDS Mutation	c.436G>A
AA Mutation	p.Gly146Arg(p.G146R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368592
Start	132784932:132784932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818C>T
AA Mutation	p.Ala273Val(p.A273V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368592
Start	132784930:132784930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820G>A
AA Mutation	p.Gly274Arg(p.G274R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368592
Start	132785045:132785045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759933944
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368592
Start	132784994:132784994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.756G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NKX6-2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368592
Start	132785056:132785056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.694G>A
AA Mutation	p.Ala232Thr(p.A232T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368592
Start	132784967:132784967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.783G>A
Mutation Classification	Silent
Feature Type	Transcript