Colon Cancer: Gene >> HTR1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961551:63961551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169G>A
AA Mutation	p.Val57Met(p.V57M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961484:63961484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236C>T
AA Mutation	p.Ala79Val(p.A79V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63960977:63960977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.743C>T
AA Mutation	p.Pro248Leu(p.P248L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961601:63961601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119C>A
AA Mutation	p.Ser40Tyr(p.S40Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961293:63961293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427G>A
AA Mutation	p.Asp143Asn(p.D143N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961526:63961526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.194G>A
AA Mutation	p.Arg65His(p.R65H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961193:63961193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527G>A
AA Mutation	p.Arg176His(p.R176H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961113:63961113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607G>A
AA Mutation	p.Ala203Thr(p.A203T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63960458:63960458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1262G>A
AA Mutation	p.Arg421His(p.R421H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63960602:63960602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118G>C
AA Mutation	p.Ser373Thr(p.S373T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961164:63961164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557845021
CDS Mutation	c.556G>A
AA Mutation	p.Ala186Thr(p.A186T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961329:63961329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391G>A
AA Mutation	p.Ala131Thr(p.A131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961532:63961532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188T>C
AA Mutation	p.Leu63Ser(p.L63S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961139:63961139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581G>C
AA Mutation	p.Gly194Ala(p.G194A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961071:63961071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649C>T
AA Mutation	p.Arg217Cys(p.R217C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961143:63961143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577C>A
AA Mutation	p.His193Asn(p.H193N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63960989:63960989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.731C>A
AA Mutation	p.Ala244Glu(p.A244E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63960841:63960841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63961336:63961336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199699351
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63961033:63961033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63961033:63961033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63960682:63960682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63960859:63960859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763855576
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63960736:63960736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200770355
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63960766:63960766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.954C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63960493:63960493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63960681:63960681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63961261:63961261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63961210:63961210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63961393:63961393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63961621:63961621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775530992
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323865
Start	63961099:63961099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.621G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HTR1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961133:63961133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587C>G
AA Mutation	p.Thr196Ser(p.T196S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63960908:63960908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812C>T
AA Mutation	p.Ala271Val(p.A271V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323865
Start	63961080:63961080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>A
AA Mutation	p.Leu214Ile(p.L214I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript