Colon Cancer: Gene >> RNASET2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000476238
Start	166931061:166931061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550T>A
AA Mutation	p.Cys184Ser(p.C184S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000476238
Start	166938961:166938961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117003826
CDS Mutation	c.380C>T
AA Mutation	p.Ala127Val(p.A127V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000476238
Start	166931093:166931093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518C>T
AA Mutation	p.Ala173Val(p.A173V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000476238
Start	166952527:166952527(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.108delA
AA Mutation	p.Lys36AsnfsTer2(p.K36Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000476238
Start	166931059:166931059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552C>A
AA Mutation	p.Cys184Ter(p.C184*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000476238
Start	166934137:166934137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.447-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RNASET2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000476238
Start	166931103:166931103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508G>T
AA Mutation	p.Asp170Tyr(p.D170Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript