Colon Cancer: Gene >> GPRC5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000014914
Start	12908892:12908892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643C>T
AA Mutation	p.Leu215Phe(p.L215F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000014914
Start	12908499:12908499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250G>C
AA Mutation	p.Ala84Pro(p.A84P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000014914
Start	12908337:12908337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775011273
CDS Mutation	c.88G>A
AA Mutation	p.Val30Ile(p.V30I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000014914
Start	12908562:12908562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313T>G
AA Mutation	p.Phe105Val(p.F105V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000014914
Start	12908619:12908619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76634522
CDS Mutation	c.370C>T
AA Mutation	p.Arg124Trp(p.R124W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000014914
Start	12912123:12912123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.962C>T
AA Mutation	p.Ser321Phe(p.S321F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000014914
Start	12908990:12908990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200045600
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000014914
Start	12908816:12908816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139349210
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000014914
Start	12908586:12908586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPRC5A

No Mutation Annotation!