Colon Cancer: Gene >> PQLC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397778
Start	79904115:79904115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677C>T
AA Mutation	p.Ala226Val(p.A226V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397778
Start	79919245:79919245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.547G>T
AA Mutation	p.Ala183Ser(p.A183S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397778
Start	79943442:79943442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224C>T
AA Mutation	p.Ser75Phe(p.S75F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397778
Start	79904036:79904036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PQLC1

No Mutation Annotation!