Colon Cancer: Gene >> RNF125

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217740
Start	32068371:32068371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686C>G
AA Mutation	p.Ser229Trp(p.S229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217740
Start	32037124:32037124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201216500
CDS Mutation	c.173G>A
AA Mutation	p.Arg58His(p.R58H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217740
Start	32037177:32037177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226C>T
AA Mutation	p.Arg76Trp(p.R76W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217740
Start	32068329:32068329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779498047
CDS Mutation	c.644G>A
AA Mutation	p.Arg215Gln(p.R215Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217740
Start	32019021:32019021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532384679
CDS Mutation	c.158G>A
AA Mutation	p.Gly53Asp(p.G53D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000217740
Start	32037194:32037196(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs778211859
CDS Mutation	c.245_247delAAG
AA Mutation	p.Glu82del(p.E82del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RNF125

No Mutation Annotation!