Colon Cancer: Gene >> GTF2H3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000543341
Start	123648066:123648066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304G>A
AA Mutation	p.Glu102Lys(p.E102K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000543341
Start	123660181:123660181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.873T>G
AA Mutation	p.Ile291Met(p.I291M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000543341
Start	123639274:123639274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.24G>T
AA Mutation	p.Leu8Phe(p.L8F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000543341
Start	123648020:123648020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773923878
CDS Mutation	c.258C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000543341
Start	123659524:123659524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780178599
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000543341
Start	123639314:123639315(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.68dupG
AA Mutation	p.Gln25AlafsTer66(p.Q25Afs*66)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GTF2H3

No Mutation Annotation!