Colon Cancer: Gene >> RNF112

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000461366
Start	19415097:19415097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186G>C
AA Mutation	p.Ala396Pro(p.A396P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000461366
Start	19414816:19414816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1055A>C
AA Mutation	p.Lys352Thr(p.K352T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000461366
Start	19414828:19414828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762130985
CDS Mutation	c.1067G>A
AA Mutation	p.Cys356Tyr(p.C356Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000461366
Start	19415846:19415846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1567G>C
AA Mutation	p.Ala523Pro(p.A523P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000461366
Start	19414857:19414857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138293491
CDS Mutation	c.1096C>T
AA Mutation	p.Arg366Trp(p.R366W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000461366
Start	19415760:19415760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369472711
CDS Mutation	c.1481G>A
AA Mutation	p.Arg494Gln(p.R494Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000461366
Start	19415332:19415332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759270591
CDS Mutation	c.1343C>T
AA Mutation	p.Pro448Leu(p.P448L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000461366
Start	19415308:19415308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1319G>T
AA Mutation	p.Arg440Met(p.R440M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000461366
Start	19415537:19415537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1370A>G
AA Mutation	p.Asp457Gly(p.D457G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RNF112

No Mutation Annotation!