Colon Cancer: Gene >> IL12B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231228
Start	159322436:159322436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.440C>T
AA Mutation	p.Thr147Ile(p.T147I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231228
Start	159322437:159322437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772801025
CDS Mutation	c.439A>G
AA Mutation	p.Thr147Ala(p.T147A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231228
Start	159316702:159316702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.970T>C
AA Mutation	p.Ser324Pro(p.S324P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231228
Start	159318793:159318793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231228
Start	159320493:159320493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771036480
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231228
Start	159323124:159323124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231228
Start	159320496:159320496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369160771
CDS Mutation	c.507G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231228
Start	159320511:159320511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231228
Start	159323214:159323214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231228
Start	159316712:159316712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752964137
CDS Mutation	c.960C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IL12B

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231228
Start	159323214:159323214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204C>A
Mutation Classification	Silent
Feature Type	Transcript