Colon Cancer: Gene >> RNF14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347642
Start	141973680:141973680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.92T>C
AA Mutation	p.Val31Ala(p.V31A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000347642
Start	141983381:141983381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1065G>T
AA Mutation	p.Glu355Asp(p.E355D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347642
Start	141978357:141978357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781535864
CDS Mutation	c.361G>A
AA Mutation	p.Val121Met(p.V121M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347642
Start	141978713:141978713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RNF14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347642
Start	141984884:141984884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762141519
CDS Mutation	c.1318G>A
AA Mutation	p.Ala440Thr(p.A440T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347642
Start	141978800:141978800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.804A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347642
Start	141980221:141980221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933G>A
Mutation Classification	Silent
Feature Type	Transcript