Colon Cancer: Gene >> RAMP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242249
Start	45183398:45183398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749634715
CDS Mutation	c.433G>A
AA Mutation	p.Asp145Asn(p.D145N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242249
Start	45183255:45183255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290A>G
AA Mutation	p.His97Arg(p.H97R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242249
Start	45183203:45183203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757054812
CDS Mutation	c.238G>A
AA Mutation	p.Val80Met(p.V80M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242249
Start	45183383:45183383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762889499
CDS Mutation	c.418C>T
AA Mutation	p.Arg140Cys(p.R140C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242249
Start	45177316:45177316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242249
Start	45183304:45183304(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763340102
CDS Mutation	c.344delC
AA Mutation	p.Pro115GlnfsTer8(p.P115Qfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RAMP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242249
Start	45183384:45183384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574497056
CDS Mutation	c.419G>A
AA Mutation	p.Arg140His(p.R140H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript