Colon Cancer: Gene >> ADCYAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000450565
Start	909594:909594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490C>A
AA Mutation	p.Gln164Lys(p.Q164K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000450565
Start	908272:908272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250G>A
AA Mutation	p.Ala84Thr(p.A84T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000450565
Start	909619:909619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515G>A
AA Mutation	p.Arg172Gln(p.R172Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000450565
Start	908266:908266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244G>T
AA Mutation	p.Asp82Tyr(p.D82Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	start_lost
Transcription ID	ENST00000450565
Start	905389:905389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3G>T
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ADCYAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000450565
Start	905474:905474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373051517
CDS Mutation	c.88G>A
AA Mutation	p.Gly30Arg(p.G30R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000450565
Start	909532:909532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428G>A
AA Mutation	p.Arg143His(p.R143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript