Colon Cancer: Gene >> TRIM47

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254816
Start	75874577:75874577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1823G>A
AA Mutation	p.Arg608Lys(p.R608K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254816
Start	75874731:75874731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763705777
CDS Mutation	c.1669C>T
AA Mutation	p.Arg557Cys(p.R557C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254816
Start	75875403:75875403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273A>G
AA Mutation	p.Lys425Glu(p.K425E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254816
Start	75874752:75874752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648G>C
AA Mutation	p.Val550Leu(p.V550L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254816
Start	75878516:75878516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254816
Start	75874543:75874543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568476297
CDS Mutation	c.1857C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254816
Start	75874507:75874507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1893C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000254816
Start	75875086:75875088(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1312_1314delGAC
AA Mutation	p.Asp438del(p.D438del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM47

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254816
Start	75875101:75875101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1299C>T
Mutation Classification	Silent
Feature Type	Transcript