Colon Cancer: Gene >> SLA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338087
Start	133038609:133038609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200951688
CDS Mutation	c.746G>A
AA Mutation	p.Arg249Gln(p.R249Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338087
Start	133060112:133060112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49C>T
AA Mutation	p.Pro17Ser(p.P17S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338087
Start	133038562:133038562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793A>G
AA Mutation	p.Ser265Gly(p.S265G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338087
Start	133045070:133045070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745463507
CDS Mutation	c.398G>A
AA Mutation	p.Arg133His(p.R133H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338087
Start	133049918:133049918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232G>T
AA Mutation	p.Ala78Ser(p.A78S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338087
Start	133050828:133050828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140863357
CDS Mutation	c.149G>A
AA Mutation	p.Arg50His(p.R50H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000338087
Start	133049923:133049923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227G>T
AA Mutation	p.Cys76Phe(p.C76F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338087
Start	133050855:133050855(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.122delC
AA Mutation	p.Pro41ArgfsTer11(p.P41Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLA

No Mutation Annotation!