Colon Cancer: Gene >> NDNF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379692
Start	121036733:121036733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1238C>A
AA Mutation	p.Pro413His(p.P413H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379692
Start	121037558:121037558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779577543
CDS Mutation	c.413C>T
AA Mutation	p.Ser138Leu(p.S138L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379692
Start	121036383:121036383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1588G>A
AA Mutation	p.Glu530Lys(p.E530K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379692
Start	121045798:121045798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40C>T
AA Mutation	p.Pro14Ser(p.P14S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379692
Start	121036327:121036327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1644A>G
AA Mutation	p.Ile548Met(p.I548M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379692
Start	121037174:121037174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375890636
CDS Mutation	c.797G>A
AA Mutation	p.Arg266His(p.R266H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379692
Start	121045787:121045787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372003668
CDS Mutation	c.51A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379692
Start	121037371:121037371(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.600delC
AA Mutation	p.Thr201LeufsTer5(p.T201Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NDNF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379692
Start	121037453:121037453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518A>G
AA Mutation	p.Tyr173Cys(p.Y173C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379692
Start	121036267:121036267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1704T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379692
Start	121045670:121045670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168C>A
Mutation Classification	Silent
Feature Type	Transcript