Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> UNC5C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95301626:95301626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470A>C
AA Mutation	p.Lys157Thr(p.K157T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95202837:95202837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2030C>T
AA Mutation	p.Ala677Val(p.A677V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95278263:95278263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590C>A
AA Mutation	p.Ala197Asp(p.A197D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95219019:95219019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1595C>G
AA Mutation	p.Ala532Gly(p.A532G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95216191:95216191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774698598
CDS Mutation	c.1666G>A
AA Mutation	p.Ala556Thr(p.A556T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95182905:95182905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139372477
CDS Mutation	c.2443G>A
AA Mutation	p.Val815Met(p.V815M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95245084:95245084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.836G>A
AA Mutation	p.Gly279Glu(p.G279E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95206644:95206644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1886C>T
AA Mutation	p.Ala629Val(p.A629V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95242447:95242447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090G>T
AA Mutation	p.Asp364Tyr(p.D364Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95242512:95242512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777156310
CDS Mutation	c.1025C>T
AA Mutation	p.Ala342Val(p.A342V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95242578:95242578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766450239
CDS Mutation	c.959C>T
AA Mutation	p.Thr320Met(p.T320M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95335516:95335516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.240C>G
AA Mutation	p.Asn80Lys(p.N80K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95278330:95278330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523G>A
AA Mutation	p.Gly175Arg(p.G175R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95219169:95219169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1445A>G
AA Mutation	p.Tyr482Cys(p.Y482C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95202838:95202838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2029G>T
AA Mutation	p.Ala677Ser(p.A677S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95335586:95335586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170C>A
AA Mutation	p.Pro57Gln(p.P57Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95206717:95206717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1813G>A
AA Mutation	p.Val605Ile(p.V605I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95220109:95220109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755116229
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95242583:95242583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.954G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95548762:95548762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.96C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95242478:95242478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201363473
CDS Mutation	c.1059C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95216162:95216162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772552427
CDS Mutation	c.1695C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95242514:95242514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746318727
CDS Mutation	c.1023G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95170309:95170309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2475G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95242481:95242481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540870072
CDS Mutation	c.1056C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95250638:95250638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000453304
Start	95170206:95170206(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2578delC
AA Mutation	p.Gln860ArgfsTer14(p.Q860Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> UNC5C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95250616:95250616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.646T>G
AA Mutation	p.Phe216Val(p.F216V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95202853:95202853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2014C>A
AA Mutation	p.His672Asn(p.H672N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95335617:95335617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139C>A
AA Mutation	p.His47Asn(p.H47N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95335435:95335435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95216165:95216165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1692C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000453304
Start	95216122:95216122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1733+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript