Colon Cancer: Gene >> HTR7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90857290:90857290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.382C>A
AA Mutation	p.Leu128Ile(p.L128I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90749122:90749122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141895642
CDS Mutation	c.1012G>A
AA Mutation	p.Val338Met(p.V338M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90743641:90743641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1345G>A
AA Mutation	p.Val449Ile(p.V449I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90749485:90749485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649C>T
AA Mutation	p.Pro217Ser(p.P217S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90857248:90857248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424G>A
AA Mutation	p.Asp142Asn(p.D142N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90748947:90748947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1187G>A
AA Mutation	p.Arg396His(p.R396H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90748976:90748976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1158C>A
AA Mutation	p.Phe386Leu(p.F386L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90749067:90749067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067C>A
AA Mutation	p.Thr356Asn(p.T356N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90749088:90749088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747084289
CDS Mutation	c.1046C>T
AA Mutation	p.Ala349Val(p.A349V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90857260:90857260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412G>A
AA Mutation	p.Val138Ile(p.V138I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90749415:90749415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768133205
CDS Mutation	c.719C>T
AA Mutation	p.Thr240Met(p.T240M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90748943:90748943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191C>A
AA Mutation	p.Ser397Arg(p.S397R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90857490:90857490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.182A>G
AA Mutation	p.Asp61Gly(p.D61G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90749139:90749139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995T>C
AA Mutation	p.Ile332Thr(p.I332T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336152
Start	90743642:90743642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1344G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336152
Start	90857435:90857435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336152
Start	90743678:90743678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1308A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336152
Start	90749015:90749015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1119C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336152
Start	90857501:90857501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HTR7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90749401:90749401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733G>A
AA Mutation	p.Ala245Thr(p.A245T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336152
Start	90743686:90743686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1300G>A
AA Mutation	p.Ala434Thr(p.A434T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336152
Start	90749075:90749075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1059C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336152
Start	90857165:90857165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507G>A
Mutation Classification	Silent
Feature Type	Transcript