Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SPN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360121
Start	29664147:29664147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756568331
CDS Mutation	c.419C>T
AA Mutation	p.Pro140Leu(p.P140L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360121
Start	29663958:29663958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230T>A
AA Mutation	p.Leu77His(p.L77H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360121
Start	29664465:29664465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181483014
CDS Mutation	c.737G>A
AA Mutation	p.Arg246Gln(p.R246Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360121
Start	29664464:29664464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.736C>T
AA Mutation	p.Arg246Trp(p.R246W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360121
Start	29664561:29664561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779631820
CDS Mutation	c.833G>A
AA Mutation	p.Arg278His(p.R278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SPN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360121
Start	29663777:29663777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>A
AA Mutation	p.Ala17Thr(p.A17T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360121
Start	29664670:29664670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360121
Start	29664139:29664139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548440370
CDS Mutation	c.411G>A
Mutation Classification	Silent
Feature Type	Transcript