Colon Cancer: Gene >> RGS19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332298
Start	64074281:64074281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Trp(p.R109W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332298
Start	64073938:64073938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762327545
CDS Mutation	c.569G>A
AA Mutation	p.Arg190Gln(p.R190Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332298
Start	64074373:64074373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.233C>T
AA Mutation	p.Thr78Met(p.T78M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332298
Start	64074270:64074270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332298
Start	64073973:64073973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769835330
CDS Mutation	c.534C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332298
Start	64073976:64073976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145585412
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332298
Start	64073988:64073988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186750098
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RGS19

No Mutation Annotation!