Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PRRT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000211413
Start	32150828:32150828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98C>T
AA Mutation	p.Pro33Leu(p.P33L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000211413
Start	32149338:32149338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805C>T
AA Mutation	p.Arg269Trp(p.R269W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000211413
Start	32150401:32150401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000211413
Start	32150872:32150872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000211413
Start	32149252:32149252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000211413
Start	32150416:32150416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147182956
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000211413
Start	32149697:32149697(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.584delG
AA Mutation	p.Gly195GlufsTer4(p.G195Efs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRRT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000211413
Start	32149253:32149253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890C>T
AA Mutation	p.Ala297Val(p.A297V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000211413
Start	32149345:32149345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript