Colon Cancer: Gene >> C14orf28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325192
Start	44900621:44900621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186C>A
AA Mutation	p.Phe62Leu(p.F62L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325192
Start	44904473:44904473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199610942
CDS Mutation	c.693T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325192
Start	44905388:44905388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325192
Start	44900530:44900530(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.99delT
AA Mutation	p.Phe33LeufsTer19(p.F33Lfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325192
Start	44900521:44900521(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.92delG
AA Mutation	p.Gly31ValfsTer21(p.G31Vfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000325192
Start	44900483:44900483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.48T>G
AA Mutation	p.Tyr16Ter(p.Y16*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> C14orf28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325192
Start	44903263:44903263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581T>G
AA Mutation	p.Phe194Cys(p.F194C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325192
Start	44900712:44900712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277C>A
AA Mutation	p.Leu93Ile(p.L93I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript