Colon Cancer: Gene >> SLC25A26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354883
Start	66346404:66346404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.494T>C
AA Mutation	p.Leu165Ser(p.L165S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354883
Start	66370534:66370534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354883
Start	66262128:66262128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354883
Start	66243211:66243211(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.204delT
AA Mutation	p.Phe68LeufsTer7(p.F68Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000354883
Start	66243307:66243307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295G>T
AA Mutation	p.Glu99Ter(p.E99*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A26

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354883
Start	66243259:66243260(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.248_249delCT
AA Mutation	p.Ser83PhefsTer27(p.S83Ffs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript