Colon Cancer: Gene >> GPR132

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329797
Start	105051229:105051229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.908C>T
AA Mutation	p.Ala303Val(p.A303V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329797
Start	105051305:105051305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832G>A
AA Mutation	p.Ala278Thr(p.A278T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329797
Start	105051629:105051629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754386954
CDS Mutation	c.508G>A
AA Mutation	p.Val170Ile(p.V170I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329797
Start	105051620:105051620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200040782
CDS Mutation	c.517G>A
AA Mutation	p.Val173Ile(p.V173I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329797
Start	105051191:105051191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200738332
CDS Mutation	c.946C>T
AA Mutation	p.Arg316Cys(p.R316C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329797
Start	105051587:105051587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550G>A
AA Mutation	p.Glu184Lys(p.E184K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329797
Start	105051600:105051600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.537G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329797
Start	105051714:105051714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537968166
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329797
Start	105051696:105051696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329797
Start	105051297:105051297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775295523
CDS Mutation	c.840C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPR132

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329797
Start	105051829:105051829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61737889
CDS Mutation	c.308G>A
AA Mutation	p.Arg103His(p.R103H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329797
Start	105051372:105051372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201367136
CDS Mutation	c.765C>T
Mutation Classification	Silent
Feature Type	Transcript