Colon Cancer: Gene >> RNASE3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304639
Start	20891705:20891705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19A>G
AA Mutation	p.Thr7Ala(p.T7A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304639
Start	20891995:20891995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.309C>A
AA Mutation	p.Phe103Leu(p.F103L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304639
Start	20891824:20891824(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.143delC
AA Mutation	p.Pro48LeufsTer31(p.P48Lfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RNASE3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304639
Start	20891874:20891874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758816325
CDS Mutation	c.188G>A
AA Mutation	p.Arg63His(p.R63H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304639
Start	20891784:20891784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371809756
CDS Mutation	c.98C>T
AA Mutation	p.Thr33Met(p.T33M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000304639
Start	20891867:20891867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183860442
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Ter(p.R61*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript