Colon Cancer: Gene >> PAOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278060
Start	133380256:133380256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760508202
CDS Mutation	c.439G>A
AA Mutation	p.Ala147Thr(p.A147T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278060
Start	133384175:133384175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763052916
CDS Mutation	c.1084C>T
AA Mutation	p.Arg362Trp(p.R362W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278060
Start	133380200:133380200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753690252
CDS Mutation	c.383C>T
AA Mutation	p.Ala128Val(p.A128V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278060
Start	133380454:133380454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637G>A
AA Mutation	p.Val213Met(p.V213M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278060
Start	133391346:133391346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1427G>A
AA Mutation	p.Arg476His(p.R476H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278060
Start	133384132:133384132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200606164
CDS Mutation	c.1041G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278060
Start	133391365:133391365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576468643
CDS Mutation	c.1446G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278060
Start	133391425:133391425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771943550
CDS Mutation	c.1506G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PAOX

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278060
Start	133384012:133384012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921G>A
Mutation Classification	Silent
Feature Type	Transcript