Colon Cancer: Gene >> RNF182

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000488300
Start	13977420:13977420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301C>A
AA Mutation	p.Leu101Met(p.L101M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000488300
Start	13977732:13977732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613G>C
AA Mutation	p.Val205Leu(p.V205L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000488300
Start	13977196:13977196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.77G>A
AA Mutation	p.Arg26Gln(p.R26Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000488300
Start	13977155:13977155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000488300
Start	13977545:13977545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528284492
CDS Mutation	c.426G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000488300
Start	13977491:13977491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752410878
CDS Mutation	c.372G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000488300
Start	13977809:13977809(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.694delT
AA Mutation	p.Cys232AlafsTer9(p.C232Afs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RNF182

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000488300
Start	13977276:13977276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.157G>T
AA Mutation	p.Asp53Tyr(p.D53Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript