Colon Cancer: Gene >> GPRC5B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300571
Start	19872095:19872095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751A>G
AA Mutation	p.Met251Val(p.M251V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300571
Start	19872565:19872565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281G>A
AA Mutation	p.Gly94Asp(p.G94D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300571
Start	19872652:19872652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.194C>A
AA Mutation	p.Ala65Glu(p.A65E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300571
Start	19872608:19872608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200327225
CDS Mutation	c.238C>T
AA Mutation	p.Arg80Trp(p.R80W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300571
Start	19872177:19872177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761585329
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300571
Start	19871877:19871877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776975656
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300571
Start	19872789:19872789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300571
Start	19872261:19872261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377381168
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300571
Start	19871922:19871922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768835018
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300571
Start	19872000:19872000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300571
Start	19872053:19872053(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.793delG
AA Mutation	p.Asp265MetfsTer143(p.D265Mfs*143)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GPRC5B

No Mutation Annotation!