Colon Cancer: Gene >> HRH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683576:175683576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343G>A
AA Mutation	p.Asp115Asn(p.D115N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175684102:175684102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367866082
CDS Mutation	c.869C>T
AA Mutation	p.Ala290Val(p.A290V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683588:175683588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Ala119Thr(p.A119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683633:175683633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400C>T
AA Mutation	p.Arg134Trp(p.R134W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683612:175683612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.379C>A
AA Mutation	p.Pro127Thr(p.P127T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175684074:175684074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841T>A
AA Mutation	p.Ser281Thr(p.S281T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683859:175683859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626C>T
AA Mutation	p.Ala209Val(p.A209V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683606:175683606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778386458
CDS Mutation	c.373C>T
AA Mutation	p.Arg125Trp(p.R125W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683927:175683927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694G>A
AA Mutation	p.Ala232Thr(p.A232T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683375:175683375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142C>T
AA Mutation	p.Arg48Trp(p.R48W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683441:175683441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208C>A
AA Mutation	p.Leu70Met(p.L70M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683639:175683639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774838699
CDS Mutation	c.406G>A
AA Mutation	p.Ala136Thr(p.A136T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683942:175683942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709G>A
AA Mutation	p.Ala237Thr(p.A237T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231683
Start	175683299:175683299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231683
Start	175684049:175684049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556155426
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HRH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175683261:175683261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28T>G
AA Mutation	p.Phe10Val(p.F10V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231683
Start	175684222:175684222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141845922
CDS Mutation	c.989G>A
AA Mutation	p.Arg330Gln(p.R330Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231683
Start	175684283:175684283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1050C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231683
Start	175683350:175683350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117C>A
Mutation Classification	Silent
Feature Type	Transcript