Colon Cancer: Gene >> B3GALT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343118
Start	39661008:39661008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449C>T
AA Mutation	p.Ala150Val(p.A150V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343118
Start	39660814:39660814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763079633
CDS Mutation	c.255G>A
AA Mutation	p.Met85Ile(p.M85I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343118
Start	39660909:39660909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350G>T
AA Mutation	p.Gly117Val(p.G117V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343118
Start	39661005:39661005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372607334
CDS Mutation	c.446C>T
AA Mutation	p.Ala149Val(p.A149V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343118
Start	39660709:39660709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777514756
CDS Mutation	c.150A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> B3GALT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343118
Start	39660836:39660836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277A>C
AA Mutation	p.Thr93Pro(p.T93P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343118
Start	39660903:39660903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344G>A
AA Mutation	p.Arg115Gln(p.R115Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343118
Start	39661237:39661237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678G>A
Mutation Classification	Silent
Feature Type	Transcript