Colon Cancer: Gene >> PTH1R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313049
Start	46902660:46902660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346C>T
AA Mutation	p.Ser449Phe(p.S449F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313049
Start	46903435:46903435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200304786
CDS Mutation	c.1561C>T
AA Mutation	p.Arg521Cys(p.R521C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313049
Start	46898185:46898185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768504854
CDS Mutation	c.536G>A
AA Mutation	p.Arg179His(p.R179H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313049
Start	46895846:46895846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290C>T
AA Mutation	p.Ala97Val(p.A97V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313049
Start	46899319:46899319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851C>T
AA Mutation	p.Ala284Val(p.A284V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313049
Start	46902618:46902618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs387907460
CDS Mutation	c.1304C>T
AA Mutation	p.Thr435Met(p.T435M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313049
Start	46893926:46893926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95T>C
AA Mutation	p.Met32Thr(p.M32T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313049
Start	46901064:46901064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028G>T
AA Mutation	p.Arg343Ile(p.R343I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000313049
Start	46898678:46898678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655C>T
AA Mutation	p.Arg219Cys(p.R219C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313049
Start	46899446:46899446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313049
Start	46901786:46901786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1137C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTH1R

No Mutation Annotation!