Colon Cancer: Gene >> A1BG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263100
Start	58352531:58352531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375725715
CDS Mutation	c.365C>T
AA Mutation	p.Ser122Leu(p.S122L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263100
Start	58347479:58347479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1354G>A
AA Mutation	p.Ala452Thr(p.A452T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263100
Start	58353114:58353114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144181716
CDS Mutation	c.154C>T
AA Mutation	p.His52Tyr(p.H52Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263100
Start	58352351:58352351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545G>A
AA Mutation	p.Cys182Tyr(p.C182Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263100
Start	58352325:58352325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540868706
CDS Mutation	c.571G>A
AA Mutation	p.Ala191Thr(p.A191T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263100
Start	58351520:58351520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770480372
CDS Mutation	c.781C>T
AA Mutation	p.Arg261Cys(p.R261C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263100
Start	58350413:58350413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263100
Start	58353426:58353426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375508010
CDS Mutation	c.12C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263100
Start	58352503:58352503(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.393delC
AA Mutation	p.Gly132AlafsTer2(p.G132Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> A1BG

No Mutation Annotation!