Colon Cancer: Gene >> ERAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254928
Start	28856525:28856525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432G>T
AA Mutation	p.Lys144Asn(p.K144N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254928
Start	28855190:28855190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156C>A
AA Mutation	p.Phe52Leu(p.F52L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254928
Start	28855221:28855221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187A>T
AA Mutation	p.Ser63Cys(p.S63C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254928
Start	28856299:28856299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319A>G
AA Mutation	p.Met107Val(p.M107V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254928
Start	28858795:28858795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931C>A
AA Mutation	p.Leu311Ile(p.L311I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254928
Start	28855040:28855040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254928
Start	28855076:28855076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254928
Start	28856322:28856323(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.342_343insT
AA Mutation	p.Arg115SerfsTer53(p.R115Sfs*53)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ERAL1

Mutation ID	1
Mutation Consequence	start_lost
Transcription ID	ENST00000254928
Start	28855036:28855036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2T>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript