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Results for "SLC2A4RG"

Variant Events: 5

Gene
Gene symbol on which the variant is located
ID
Subject Identifier from the original study
Location
Genomic location of the reference allele
REF
Reference allele
ALT
Alternate allele
Context
Variant functional categories
Variant validation performed by an orthogonal method and reported
Inheritance
Reported inheritance status
Effects
Variant effect on transcript per Annovar
Transcript
Transcript used for the cDNA/Protein mutation
cDNA
cDNA variant notation
Protein
Protein variant notation
CADD-Phred v1.0
CADD phred-like score. This is phred-like rank score based on whole genome CADD raw scores
ExAC v0.3
ExAC population frequency (version 0.3)
Sources
Source(s) where variants from this event are reported
SLC2A4RG     JASD_Fam0096chr20:
62373543-62373543
GAexonicDe novononsynonymous SNVNM_020062c.G640Ap.A214T10.59-Takata2018 E
SLC2A4RG     MSSNG00077-005chr20:
62373773-62373773
CTexonicDe novosynonymous SNVNM_020062c.C765Tp.D255D-3.342E-5Trost2022 G
SLC2A4RG     SP0143782chr20:
62371206-62371206
GCdownstream;upstreamDe novo--Fu2022 E
Trost2022 G
Trost2022 G
SLC2A4RG     mAGRE4435chr20:
62373577-62373594
ACCTGGGGTGCGGCGGGGAexonicPaternalnonframeshift deletionNM_020062c.675_680delp.225_227del-4.0E-4Cirnigliaro2023 G
SLC2A4RG     SP0132441chr20:
62371871-62371871
GAexonicDe novononsynonymous SNVNM_020062c.G268Ap.V90I12.14-Fu2022 E
Trost2022 G
Zhou2022 GE
Source Variant Information

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Source:

Paper alias:

No records found.
Paper Information
Title
Authors
Technology
Variant source
Cohorts
Design
URL
Pubmed
Subject count
The number of subjects for this study could not be determined directly from the variant data; the value given is that reported by the authors in the publication.
Variant event count
Curation notesView
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