Colon Cancer: Gene >> APBA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316757
Start	3754308:3754308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649G>T
AA Mutation	p.Asp217Tyr(p.D217Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316757
Start	3759912:3759912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353G>A
AA Mutation	p.Cys118Tyr(p.C118Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316757
Start	3751517:3751517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376088061
CDS Mutation	c.1432G>A
AA Mutation	p.Val478Ile(p.V478I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316757
Start	3754078:3754078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790A>G
AA Mutation	p.Thr264Ala(p.T264A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316757
Start	3751320:3751320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1525C>T
AA Mutation	p.Leu509Phe(p.L509F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316757
Start	3760152:3760152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113A>G
AA Mutation	p.Asp38Gly(p.D38G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000316757
Start	3752516:3752516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575676926
CDS Mutation	c.1387G>A
AA Mutation	p.Ala463Thr(p.A463T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316757
Start	3751533:3751533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112086597
CDS Mutation	c.1416G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316757
Start	3760133:3760133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749259377
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316757
Start	3760058:3760058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61729800
CDS Mutation	c.207C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316757
Start	3759856:3759856(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.409delC
AA Mutation	p.Arg137AspfsTer45(p.R137Dfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> APBA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316757
Start	3759900:3759900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201048764
CDS Mutation	c.365C>T
AA Mutation	p.Pro122Leu(p.P122L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316757
Start	3752952:3752952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367941981
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript