Colon Cancer: Gene >> GPRC5C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392627
Start	74446888:74446888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139477313
CDS Mutation	c.1321G>A
AA Mutation	p.Ala441Thr(p.A441T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392627
Start	74439910:74439910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551384896
CDS Mutation	c.269G>A
AA Mutation	p.Arg90His(p.R90H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392627
Start	74443905:74443905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274A>C
AA Mutation	p.Lys425Thr(p.K425T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392627
Start	74446928:74446928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144516528
CDS Mutation	c.1361G>A
AA Mutation	p.Arg454Gln(p.R454Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392627
Start	74440317:74440317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374834578
CDS Mutation	c.676C>T
AA Mutation	p.Arg226Trp(p.R226W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392627
Start	74439842:74439842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201G>T
AA Mutation	p.Trp67Cys(p.W67C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392627
Start	74440328:74440328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392627
Start	74440820:74440820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392627
Start	74432089:74432089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392627
Start	74440670:74440670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764963013
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392627
Start	74439872:74439872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392627
Start	74443885:74443885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392627
Start	74432113:74432113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392627
Start	74440223:74440223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371327877
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPRC5C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392627
Start	74440329:74440329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751199319
CDS Mutation	c.688G>A
AA Mutation	p.Glu230Lys(p.E230K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392627
Start	74440465:74440465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824C>A
AA Mutation	p.Ala275Asp(p.A275D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392627
Start	74440533:74440533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775061799
CDS Mutation	c.892G>A
AA Mutation	p.Val298Ile(p.V298I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript