Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SDC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302190
Start	96609535:96609535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593A>G
AA Mutation	p.Glu198Gly(p.E198G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302190
Start	96494297:96494297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26C>G
AA Mutation	p.Thr9Ser(p.T9S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302190
Start	96608401:96608401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200028820
CDS Mutation	c.373G>A
AA Mutation	p.Glu125Lys(p.E125K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302190
Start	96609464:96609464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.522G>T
AA Mutation	p.Lys174Asn(p.K174N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302190
Start	96609451:96609451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774751152
CDS Mutation	c.509G>A
AA Mutation	p.Arg170His(p.R170H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302190
Start	96608400:96608400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766386558
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302190
Start	96609545:96609545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770229518
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SDC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302190
Start	96609421:96609421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479C>A
AA Mutation	p.Ala160Glu(p.A160E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302190
Start	96609451:96609451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774751152
CDS Mutation	c.509G>A
AA Mutation	p.Arg170His(p.R170H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302190
Start	96609414:96609414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.472C>A
AA Mutation	p.Leu158Ile(p.L158I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript