Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MGLL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398104
Start	127695133:127695133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138122374
CDS Mutation	c.628G>A
AA Mutation	p.Gly210Ser(p.G210S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398104
Start	127710655:127710655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374353919
CDS Mutation	c.491C>T
AA Mutation	p.Ala164Val(p.A164V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398104
Start	127721127:127721127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406C>T
AA Mutation	p.Pro136Ser(p.P136S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398104
Start	127710594:127710594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538109563
CDS Mutation	c.552C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398104
Start	127710635:127710635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398104
Start	127695064:127695064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398104
Start	127722550:127722550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754529528
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MGLL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398104
Start	127781802:127781802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>G
AA Mutation	p.Phe73Leu(p.F73L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398104
Start	127781866:127781866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.155G>A
AA Mutation	p.Gly52Glu(p.G52E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398104
Start	127722558:127722558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778074591
CDS Mutation	c.241G>A
AA Mutation	p.Gly81Arg(p.G81R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript