Colon Cancer: Gene >> GLDN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335449
Start	51404464:51404464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1366A>G
AA Mutation	p.Thr456Ala(p.T456A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335449
Start	51404384:51404384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286T>C
AA Mutation	p.Val429Ala(p.V429A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335449
Start	51404636:51404636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1538C>T
AA Mutation	p.Ser513Phe(p.S513F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335449
Start	51404653:51404653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1555A>T
AA Mutation	p.Met519Leu(p.M519L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335449
Start	51404541:51404541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1443C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000335449
Start	51404338:51404338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539703340
CDS Mutation	c.1240C>T
AA Mutation	p.Arg414Ter(p.R414*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GLDN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335449
Start	51400212:51400212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838A>C
AA Mutation	p.Asn280His(p.N280H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript