Colon Cancer: Gene >> B4GALT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379731
Start	33113817:33113817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021A>G
AA Mutation	p.Ile341Val(p.I341V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379731
Start	33120553:33120553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702A>C
AA Mutation	p.Glu234Asp(p.E234D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379731
Start	33120444:33120444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750802296
CDS Mutation	c.811G>A
AA Mutation	p.Val271Ile(p.V271I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379731
Start	33113801:33113801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1037A>G
AA Mutation	p.Asp346Gly(p.D346G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379731
Start	33166815:33166815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355G>A
AA Mutation	p.Val119Met(p.V119M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379731
Start	33116032:33116032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918T>G
AA Mutation	p.Asn306Lys(p.N306K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379731
Start	33120440:33120440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.815C>T
AA Mutation	p.Ala272Val(p.A272V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379731
Start	33113460:33113460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762140480
CDS Mutation	c.1191G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379731
Start	33116086:33116086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.864T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379731
Start	33113481:33113481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1170C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379731
Start	33120465:33120465(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.790delT
AA Mutation	p.Ser264HisfsTer29(p.S264Hfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> B4GALT1

No Mutation Annotation!