Colon Cancer: Gene >> CLEC14A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38255684:38255684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339C>A
AA Mutation	p.Phe113Leu(p.F113L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38255653:38255653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>A
AA Mutation	p.Glu124Lys(p.E124K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38255329:38255329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694G>A
AA Mutation	p.Gly232Ser(p.G232S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38254609:38254609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414C>T
AA Mutation	p.Arg472Trp(p.R472W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38255445:38255445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578G>A
AA Mutation	p.Arg193His(p.R193H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38255302:38255302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721G>A
AA Mutation	p.Asp241Asn(p.D241N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38255215:38255215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808G>A
AA Mutation	p.Ala270Thr(p.A270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38254581:38254581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1442C>T
AA Mutation	p.Ala481Val(p.A481V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38255530:38255530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11553024
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Cys(p.R165C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38254625:38254625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1398C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38255285:38255285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38255336:38255336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38255741:38255741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38256014:38256014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38255498:38255498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38255537:38255537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38255594:38255594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38254871:38254871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1152T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38255054:38255054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772963880
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38255330:38255330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CLEC14A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38254993:38254993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030C>T
AA Mutation	p.Pro344Ser(p.P344S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38255668:38255668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Asp119Asn(p.D119N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342213
Start	38255109:38255109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914G>A
AA Mutation	p.Arg305His(p.R305H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38255084:38255084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765743832
CDS Mutation	c.939C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38254592:38254592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342213
Start	38255291:38255291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.732T>C
Mutation Classification	Silent
Feature Type	Transcript