Colon Cancer: Gene >> RNASEH2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336617
Start	50956458:50956458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923A>C
AA Mutation	p.Lys308Thr(p.K308T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336617
Start	50929479:50929479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.141A>C
AA Mutation	p.Glu47Asp(p.E47D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336617
Start	50945473:50945473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557G>A
AA Mutation	p.Ser186Asn(p.S186N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336617
Start	50927471:50927471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199839728
CDS Mutation	c.129C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336617
Start	50934941:50934941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RNASEH2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336617
Start	50945460:50945460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544A>G
AA Mutation	p.Asn182Asp(p.N182D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336617
Start	50953914:50953914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336617
Start	50956432:50956433(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.903dupT
AA Mutation	p.Gly302TrpfsTer5(p.G302Wfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript