Colon Cancer: Gene >> HTR6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289753
Start	19666162:19666162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.409C>T
AA Mutation	p.Arg137Cys(p.R137C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289753
Start	19666351:19666351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598C>T
AA Mutation	p.Pro200Ser(p.P200S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289753
Start	19666355:19666355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.602C>T
AA Mutation	p.Ser201Leu(p.S201L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000289753
Start	19678637:19678637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.785A>G
AA Mutation	p.Lys262Arg(p.K262R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000289753
Start	19678986:19678986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775112428
CDS Mutation	c.941C>T
AA Mutation	p.Thr314Ile(p.T314I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000289753
Start	19679337:19679337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376637765
CDS Mutation	c.1292G>A
AA Mutation	p.Arg431Gln(p.R431Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289753
Start	19665897:19665897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.144C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289753
Start	19679065:19679065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1020T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289753
Start	19666110:19666110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HTR6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289753
Start	19665962:19665962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.209C>T
AA Mutation	p.Thr70Met(p.T70M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289753
Start	19679035:19679035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149152488
CDS Mutation	c.990G>A
Mutation Classification	Silent
Feature Type	Transcript