Colon Cancer: Gene >> ATAD3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378755
Start	1527847:1527847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1634C>G
AA Mutation	p.Ala545Gly(p.A545G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378755
Start	1522838:1522838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540171241
CDS Mutation	c.989C>T
AA Mutation	p.Pro330Leu(p.P330L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378755
Start	1520249:1520249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776584627
CDS Mutation	c.767G>A
AA Mutation	p.Arg256His(p.R256H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378755
Start	1523544:1523544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779111850
CDS Mutation	c.1084G>A
AA Mutation	p.Ala362Thr(p.A362T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378755
Start	1524324:1524324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285G>A
AA Mutation	p.Val429Met(p.V429M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378755
Start	1533930:1533930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769976477
CDS Mutation	c.1763C>T
AA Mutation	p.Thr588Met(p.T588M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378755
Start	1529274:1529274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1701T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000378755
Start	1525239:1525239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1359-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ATAD3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378755
Start	1523869:1523869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138G>A
AA Mutation	p.Ala380Thr(p.A380T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378755
Start	1527734:1527734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs74047254
CDS Mutation	c.1521C>T
Mutation Classification	Silent
Feature Type	Transcript