Colon Cancer: Gene >> HNRNPLL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000449105
Start	38585828:38585828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362T>C
AA Mutation	p.Ile121Thr(p.I121T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000449105
Start	38591543:38591543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295T>A
AA Mutation	p.Phe99Ile(p.F99I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000449105
Start	38602457:38602457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170G>A
AA Mutation	p.Gly57Asp(p.G57D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449105
Start	38583912:38583912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000449105
Start	38591597:38591597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241C>T
AA Mutation	p.Arg81Ter(p.R81*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPLL

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449105
Start	38585761:38585761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429T>C
Mutation Classification	Silent
Feature Type	Transcript