Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SORCS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7718095:7718095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778344671
CDS Mutation	c.2336C>T
AA Mutation	p.Pro779Leu(p.P779L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7664364:7664364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371719399
CDS Mutation	c.964G>A
AA Mutation	p.Val322Ile(p.V322I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7737088:7737088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762210472
CDS Mutation	c.3331G>A
AA Mutation	p.Val1111Met(p.V1111M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7689564:7689564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191021957
CDS Mutation	c.1567G>A
AA Mutation	p.Ala523Thr(p.A523T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7704272:7704272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201433688
CDS Mutation	c.1856C>T
AA Mutation	p.Thr619Met(p.T619M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000507866
Start	7396289:7396289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.482T>A
AA Mutation	p.Val161Glu(p.V161E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7718052:7718052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2293G>T
AA Mutation	p.Asp765Tyr(p.D765Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7676093:7676093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1205C>T
AA Mutation	p.Ala402Val(p.A402V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7729650:7729650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759118679
CDS Mutation	c.3046G>A
AA Mutation	p.Asp1016Asn(p.D1016N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7726880:7726880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2846A>C
AA Mutation	p.Asp949Ala(p.D949A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7728355:7728355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2875T>G
AA Mutation	p.Phe959Val(p.F959V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7714277:7714277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748086651
CDS Mutation	c.2027G>A
AA Mutation	p.Arg676Gln(p.R676Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7718016:7718016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777090653
CDS Mutation	c.2257C>T
AA Mutation	p.Arg753Trp(p.R753W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7689532:7689532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1535A>G
AA Mutation	p.Tyr512Cys(p.Y512C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7638359:7638359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35727450
CDS Mutation	c.680G>A
AA Mutation	p.Arg227Gln(p.R227Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7664358:7664358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747884144
CDS Mutation	c.958C>T
AA Mutation	p.Arg320Trp(p.R320W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7676069:7676069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1181C>G
AA Mutation	p.Thr394Arg(p.T394R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7703319:7703319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764411472
CDS Mutation	c.1708G>A
AA Mutation	p.Gly570Ser(p.G570S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507866
Start	7638426:7638426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507866
Start	7728429:7728429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551349051
CDS Mutation	c.2949C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507866
Start	7718156:7718156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375585366
CDS Mutation	c.2397C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507866
Start	7676160:7676160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775480246
CDS Mutation	c.1272C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507866
Start	7664414:7664414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114808144
CDS Mutation	c.1014C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SORCS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7676218:7676218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1330G>A
AA Mutation	p.Asp444Asn(p.D444N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7396291:7396291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484A>T
AA Mutation	p.Ile162Phe(p.I162F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000507866
Start	7715310:7715310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2251G>T
AA Mutation	p.Gly751Trp(p.G751W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7664358:7664358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747884144
CDS Mutation	c.958C>T
AA Mutation	p.Arg320Trp(p.R320W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000507866
Start	7664415:7664415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192102940
CDS Mutation	c.1015G>A
AA Mutation	p.Ala339Thr(p.A339T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000507866
Start	7396355:7396355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548G>A
AA Mutation	p.Arg183Gln(p.R183Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507866
Start	7396305:7396305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498G>A
Mutation Classification	Silent
Feature Type	Transcript