Colon Cancer: Gene >> HRH3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000340177
Start	62218655:62218655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747290921
CDS Mutation	c.253G>A
AA Mutation	p.Ala85Thr(p.A85T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340177
Start	62218561:62218561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.347T>G
AA Mutation	p.Leu116Arg(p.L116R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340177
Start	62216839:62216839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505C>T
AA Mutation	p.Pro169Ser(p.P169S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340177
Start	62216655:62216655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751534866
CDS Mutation	c.689G>A
AA Mutation	p.Arg230His(p.R230H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340177
Start	62216053:62216053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291A>C
AA Mutation	p.Lys431Gln(p.K431Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340177
Start	62216060:62216060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201271584
CDS Mutation	c.1284C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HRH3

No Mutation Annotation!