Colon Cancer: Gene >> TDGF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296145
Start	46579971:46579971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359A>T
AA Mutation	p.His120Leu(p.H120L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296145
Start	46579967:46579967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200480549
CDS Mutation	c.355C>T
AA Mutation	p.Pro119Ser(p.P119S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296145
Start	46579807:46579807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>A
AA Mutation	p.Pro98Thr(p.P98T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296145
Start	46579969:46579969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.357C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296145
Start	46579134:46579134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296145
Start	46581193:46581193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510A>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TDGF1

Mutation ID	1
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000296145
Start	46579367:46579368(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.223+2dupT
Mutation Classification	Splice_Site
Feature Type	Transcript