Colon Cancer: Gene >> TECR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215567
Start	14563218:14563218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763449006
CDS Mutation	c.79G>A
AA Mutation	p.Ala27Thr(p.A27T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215567
Start	14565843:14565843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899G>A
AA Mutation	p.Arg300His(p.R300H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000215567
Start	14564220:14564220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Arg141His(p.R141H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215567
Start	14565119:14565119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215567
Start	14563217:14563217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776029034
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TECR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215567
Start	14564066:14564066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352G>T
AA Mutation	p.Asp118Tyr(p.D118Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215567
Start	14564809:14564809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759825452
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript