Colon Cancer: Gene >> HAGH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397356
Start	1817185:1817185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148679753
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Trp(p.R210W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397356
Start	1819922:1819922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.407A>G
AA Mutation	p.Lys136Arg(p.K136R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397356
Start	1820001:1820001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772821746
CDS Mutation	c.328G>A
AA Mutation	p.Gly110Arg(p.G110R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397356
Start	1822940:1822940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397356
Start	1822336:1822337(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.277dupG
AA Mutation	p.Val93GlyfsTer20(p.V93Gfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HAGH

No Mutation Annotation!