Colon Cancer: Gene >> LGALS3BP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262776
Start	78976127:78976127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82G>A
AA Mutation	p.Asp28Asn(p.D28N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262776
Start	78974775:78974775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771490373
CDS Mutation	c.289G>A
AA Mutation	p.Glu97Lys(p.E97K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262776
Start	78972084:78972084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250T>C
AA Mutation	p.Phe417Ser(p.F417S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262776
Start	78974688:78974688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376G>A
AA Mutation	p.Glu126Lys(p.E126K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262776
Start	78971676:78971676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143986382
CDS Mutation	c.1658C>T
AA Mutation	p.Ser553Leu(p.S553L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262776
Start	78971824:78971824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1510C>A
AA Mutation	p.Leu504Met(p.L504M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262776
Start	78976119:78976119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11548452
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262776
Start	78972326:78972326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536183507
CDS Mutation	c.1008T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LGALS3BP

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262776
Start	78972359:78972359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975G>A
Mutation Classification	Silent
Feature Type	Transcript