Colon Cancer: Gene >> TFDP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310125
Start	133217326:133217326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934G>A
AA Mutation	p.Glu312Lys(p.E312K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310125
Start	133217845:133217845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415G>A
AA Mutation	p.Ala139Thr(p.A139T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310125
Start	133218166:133218166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94T>A
AA Mutation	p.Ser32Thr(p.S32T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310125
Start	133217170:133217170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090G>A
AA Mutation	p.Gly364Arg(p.G364R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310125
Start	133217263:133217263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997G>A
AA Mutation	p.Ala333Thr(p.A333T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310125
Start	133217102:133217102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1158G>T
AA Mutation	p.Glu386Asp(p.E386D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310125
Start	133218125:133218125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.135C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310125
Start	133217441:133217441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762868660
CDS Mutation	c.819C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310125
Start	133217174:133217174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1086G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TFDP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310125
Start	133217818:133217818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765029523
CDS Mutation	c.442G>A
AA Mutation	p.Ala148Thr(p.A148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310125
Start	133217340:133217340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920G>A
AA Mutation	p.Gly307Glu(p.G307E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript