Colon Cancer: Gene >> RGS14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000408923
Start	177366262:177366262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153C>A
AA Mutation	p.Ser51Arg(p.S51R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000408923
Start	177366218:177366218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374571122
CDS Mutation	c.109C>T
AA Mutation	p.Arg37Cys(p.R37C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000408923
Start	177367440:177367440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510C>A
AA Mutation	p.Ser170Arg(p.S170R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000408923
Start	177367502:177367502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572G>A
AA Mutation	p.Arg191His(p.R191H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000408923
Start	177370919:177370919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142C>T
AA Mutation	p.Ala381Val(p.A381V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000408923
Start	177367511:177367511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581G>A
AA Mutation	p.Arg194Gln(p.R194Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000408923
Start	177367717:177367717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631C>T
AA Mutation	p.Pro211Ser(p.P211S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000408923
Start	177366312:177366312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.203T>A
AA Mutation	p.Phe68Tyr(p.F68Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000408923
Start	177366290:177366290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753166092
CDS Mutation	c.181G>A
AA Mutation	p.Val61Met(p.V61M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408923
Start	177371907:177371907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774072163
CDS Mutation	c.1533C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408923
Start	177372042:177372042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1668A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408923
Start	177366941:177366941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200942382
CDS Mutation	c.390G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000408923
Start	177367498:177367498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568G>T
AA Mutation	p.Gly190Ter(p.G190*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RGS14

No Mutation Annotation!