Colon Cancer: Gene >> SLC25A19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320362
Start	75278295:75278295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500G>T
AA Mutation	p.Arg167Met(p.R167M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320362
Start	75283454:75283454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372219499
CDS Mutation	c.428G>A
AA Mutation	p.Arg143His(p.R143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320362
Start	75273635:75273635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200977389
CDS Mutation	c.779G>A
AA Mutation	p.Arg260Gln(p.R260Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320362
Start	75283483:75283483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320362
Start	75278306:75278306(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.489delG
AA Mutation	p.Thr164ProfsTer19(p.T164Pfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320362
Start	75286371:75286371(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.221delG
AA Mutation	p.Gly74ValfsTer17(p.G74Vfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A19

No Mutation Annotation!