Colon Cancer: Gene >> RNF128

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255499
Start	106785113:106785113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750124343
CDS Mutation	c.781C>T
AA Mutation	p.Arg261Cys(p.R261C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255499
Start	106795616:106795616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1190C>A
AA Mutation	p.Ser397Tyr(p.S397Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255499
Start	106727141:106727141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255499
Start	106726967:106726967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255499
Start	106787929:106787929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255499
Start	106791133:106791133(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1053delC
AA Mutation	p.Ser352ProfsTer40(p.S352Pfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255499
Start	106727023:106727023(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.115delG
AA Mutation	p.Ala39LeufsTer20(p.A39Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324342
Start	106694026:106694026(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs757038390
CDS Mutation	c.31delT
AA Mutation	p.Trp11GlyfsTer4(p.W11Gfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000255499
Start	106727260:106727260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.347G>A
AA Mutation	p.Trp116Ter(p.W116*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000255499
Start	106795699:106795699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273G>T
AA Mutation	p.Glu425Ter(p.E425*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324342
Start	106694312:106694313(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.316dupA
AA Mutation	p.Ile106AsnfsTer10(p.I106Nfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000255499
Start	106791222:106791223(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1141_1142insCTT
AA Mutation	p.Val381delinsAlaLeu(p.V381delinsAL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RNF128

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255499
Start	106727113:106727113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.200A>T
AA Mutation	p.Glu67Val(p.E67V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript