Colon Cancer: Gene >> EXT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343631
Start	44198007:44198007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1484A>G
AA Mutation	p.Asn495Ser(p.N495S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343631
Start	44107862:44107862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138982530
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343631
Start	44108132:44108132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.420T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343631
Start	44234219:44234219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748445132
CDS Mutation	c.1911C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343631
Start	44108162:44108162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.450C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343631
Start	44244176:44244176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2046A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343631
Start	44126872:44126872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142692757
CDS Mutation	c.996C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343631
Start	44107951:44107951(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.244delG
AA Mutation	p.Asp82IlefsTer30(p.D82Ifs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343631
Start	44206844:44206844(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1550delA
AA Mutation	p.Asn517ThrfsTer3(p.N517Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EXT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343631
Start	44124848:44124848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803A>G
AA Mutation	p.Asp268Gly(p.D268G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript