Colon Cancer: Gene >> SPDEF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374037
Start	34541046:34541046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572T>C
AA Mutation	p.Phe191Ser(p.F191S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374037
Start	34539358:34539358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721G>A
AA Mutation	p.Asp241Asn(p.D241N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374037
Start	34539295:34539295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784C>T
AA Mutation	p.Pro262Ser(p.P262S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374037
Start	34544383:34544383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375427681
CDS Mutation	c.73C>T
AA Mutation	p.Arg25Trp(p.R25W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374037
Start	34544106:34544106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350A>G
AA Mutation	p.His117Arg(p.H117R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374037
Start	34544150:34544150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748202781
CDS Mutation	c.306G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374037
Start	34544288:34544288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2233638
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374037
Start	34541108:34541108(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.510delC
AA Mutation	p.Met171TrpfsTer45(p.M171Wfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SPDEF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374037
Start	34544053:34544053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146713427
CDS Mutation	c.403G>A
AA Mutation	p.Glu135Lys(p.E135K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript