Colon Cancer: Gene >> MLNR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218721
Start	49222195:49222195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057A>G
AA Mutation	p.Ile353Val(p.I353V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218721
Start	49220559:49220559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222C>G
AA Mutation	p.Asn74Lys(p.N74K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000218721
Start	49220903:49220903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.566C>T
AA Mutation	p.Pro189Leu(p.P189L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000218721
Start	49220536:49220536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769275756
CDS Mutation	c.199C>T
AA Mutation	p.Arg67Trp(p.R67W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000218721
Start	49220870:49220870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533G>A
AA Mutation	p.Gly178Asp(p.G178D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218721
Start	49220871:49220871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.534C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218721
Start	49220919:49220919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218721
Start	49222320:49222320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1182T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218721
Start	49220655:49220655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MLNR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218721
Start	49220821:49220821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484C>A
AA Mutation	p.Leu162Ile(p.L162I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript