Colon Cancer: Gene >> SNRPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243563
Start	40759542:40759542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.358G>A
AA Mutation	p.Ala120Thr(p.A120T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243563
Start	40765087:40765087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.769G>A
AA Mutation	p.Ala257Thr(p.A257T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000243563
Start	40759609:40759609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775580802
CDS Mutation	c.425C>T
AA Mutation	p.Pro142Leu(p.P142L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000243563
Start	40757397:40757397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368973112
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Trp(p.R47W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243563
Start	40759565:40759565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374319458
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243563
Start	40759576:40759576(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.396delC
AA Mutation	p.Val133TrpfsTer15(p.V133Wfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SNRPA

No Mutation Annotation!