Colon Cancer: Gene >> HRH4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256906
Start	24476916:24476916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527C>G
AA Mutation	p.Ala176Gly(p.A176G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256906
Start	24477540:24477540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1151A>G
AA Mutation	p.His384Arg(p.H384R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256906
Start	24477309:24477309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920T>A
AA Mutation	p.Ile307Asn(p.I307N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256906
Start	24477398:24477398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009T>A
AA Mutation	p.Ser337Thr(p.S337T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256906
Start	24476781:24476781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.392A>C
AA Mutation	p.Lys131Thr(p.K131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000256906
Start	24476960:24476960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773632780
CDS Mutation	c.571G>A
AA Mutation	p.Ala191Thr(p.A191T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256906
Start	24476890:24476890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501A>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HRH4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256906
Start	24477112:24477112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372177844
CDS Mutation	c.723G>A
Mutation Classification	Silent
Feature Type	Transcript