Colon Cancer: Gene >> REPS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357277
Start	17006323:17006323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772735900
CDS Mutation	c.376C>T
AA Mutation	p.Arg126Trp(p.R126W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357277
Start	17006272:17006272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325T>C
AA Mutation	p.Phe109Leu(p.F109L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357277
Start	17147461:17147461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750209945
CDS Mutation	c.1963C>T
AA Mutation	p.Arg655Cys(p.R655C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357277
Start	17068429:17068429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1237C>A
AA Mutation	p.Leu413Ile(p.L413I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357277
Start	17062525:17062525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144817649
CDS Mutation	c.1202G>A
AA Mutation	p.Arg401Gln(p.R401Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357277
Start	17062455:17062455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1132T>C
AA Mutation	p.Trp378Arg(p.W378R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357277
Start	17054825:17054825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989A>G
AA Mutation	p.Asp330Gly(p.D330G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357277
Start	17054892:17054892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762688027
CDS Mutation	c.1056C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> REPS2

No Mutation Annotation!