Colon Cancer: Gene >> RNF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373479
Start	37360563:37360563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229A>G
AA Mutation	p.Met77Val(p.M77V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373479
Start	37369105:37369105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.862A>C
AA Mutation	p.Met288Leu(p.M288L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373479
Start	37369092:37369092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.849G>T
AA Mutation	p.Lys283Asn(p.K283N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373479
Start	37374657:37374657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1076A>C
AA Mutation	p.Lys359Thr(p.K359T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373479
Start	37368613:37368613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>A
AA Mutation	p.Val124Ile(p.V124I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373479
Start	37368874:37368874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631G>C
AA Mutation	p.Glu211Gln(p.E211Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373479
Start	37381289:37381289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1376A>C
AA Mutation	p.Lys459Thr(p.K459T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373479
Start	37368746:37368746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759453955
CDS Mutation	c.503G>A
AA Mutation	p.Gly168Asp(p.G168D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373479
Start	37376956:37376956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769385134
CDS Mutation	c.1159G>A
AA Mutation	p.Glu387Lys(p.E387K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373479
Start	37368677:37368677(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.440delA
AA Mutation	p.Asn147IlefsTer4(p.N147Ifs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000373479
Start	37360458:37360458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124C>T
AA Mutation	p.Arg42Ter(p.R42*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000373479
Start	37390741:37390741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1442-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RNF8

No Mutation Annotation!