Colon Cancer: Gene >> MLST8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397124
Start	2206389:2206389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161G>A
AA Mutation	p.Arg54His(p.R54H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397124
Start	2206582:2206582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397124
Start	2206627:2206627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766765908
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397124
Start	2207074:2207074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758000683
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397124
Start	2207261:2207261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397124
Start	2207300:2207300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.528C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	start_lost
Transcription ID	ENST00000397124
Start	2206087:2206087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MLST8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397124
Start	2206573:2206573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258G>T
AA Mutation	p.Lys86Asn(p.K86N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397124
Start	2207258:2207258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185180342
CDS Mutation	c.486C>T
Mutation Classification	Silent
Feature Type	Transcript