Colon Cancer: Gene >> DIRC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261038
Start	122856364:122856364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1000G>A
AA Mutation	p.Ala334Thr(p.A334T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261038
Start	122826858:122826858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496G>A
AA Mutation	p.Ala166Thr(p.A166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261038
Start	122827006:122827006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.644T>G
AA Mutation	p.Leu215Arg(p.L215R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261038
Start	122872464:122872464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150962928
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DIRC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261038
Start	122860128:122860128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763882530
CDS Mutation	c.1064C>T
AA Mutation	p.Ser355Leu(p.S355L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000261038
Start	122845770:122845770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746632002
CDS Mutation	c.841C>T
AA Mutation	p.Arg281Ter(p.R281*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript