Colon Cancer: Gene >> SUV39H1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376687
Start	48706564:48706564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1042G>A
AA Mutation	p.Ala348Thr(p.A348T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376687
Start	48706310:48706310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201867779
CDS Mutation	c.874C>T
AA Mutation	p.Arg292Cys(p.R292C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376687
Start	48707464:48707464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782387231
CDS Mutation	c.1133G>A
AA Mutation	p.Arg378His(p.R378H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376687
Start	48700559:48700559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782300985
CDS Mutation	c.634C>T
AA Mutation	p.Arg212Trp(p.R212W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376687
Start	48698939:48698939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376687
Start	48700297:48700297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376687
Start	48700744:48700744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782397110
CDS Mutation	c.819C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376687
Start	48706273:48706273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376687
Start	48700513:48700513(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.592delG
AA Mutation	p.Ala198ArgfsTer140(p.A198Rfs*140)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SUV39H1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376687
Start	48706536:48706536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1014C>A
AA Mutation	p.Asp338Glu(p.D338E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript