Colon Cancer: Gene >> HNRNPH3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265866
Start	68341208:68341208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.674T>C
AA Mutation	p.Ile225Thr(p.I225T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265866
Start	68337255:68337255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34G>A
AA Mutation	p.Asp12Asn(p.D12N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265866
Start	68338673:68338673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422A>C
AA Mutation	p.Asp141Ala(p.D141A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265866
Start	68341601:68341601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265866
Start	68337275:68337275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000265866
Start	68338660:68338660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.409C>T
AA Mutation	p.Arg137Ter(p.R137*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPH3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265866
Start	68338676:68338676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425G>A
AA Mutation	p.Gly142Glu(p.G142E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript