Colon Cancer: Gene >> RAMP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253796
Start	42762361:42762361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369493002
CDS Mutation	c.170C>T
AA Mutation	p.Thr57Met(p.T57M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253796
Start	42762443:42762443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753752218
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253796
Start	42762778:42762779(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.459dupC
AA Mutation	p.Ile154HisfsTer16(p.I154Hfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000253796
Start	42762354:42762354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.168delG
AA Mutation	p.Thr57ArgfsTer2(p.X56_splice)
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RAMP2

No Mutation Annotation!