Colon Cancer: Gene >> TCF21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000237316
Start	133889530:133889530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745627463
CDS Mutation	c.133G>A
AA Mutation	p.Glu45Lys(p.E45K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000237316
Start	133889662:133889662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>G
AA Mutation	p.Arg89Gly(p.R89G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000237316
Start	133889608:133889608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750251328
CDS Mutation	c.211G>A
AA Mutation	p.Gly71Arg(p.G71R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237316
Start	133889583:133889583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237316
Start	133889706:133889706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.309G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TCF21

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237316
Start	133889742:133889742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761923325
CDS Mutation	c.345C>T
Mutation Classification	Silent
Feature Type	Transcript