RGD:401926996 Rat Genome Database

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Variant: RGD:401926996 -  Homo sapiens

RGD ID: 401926996
ClinVar ID: CV2828920
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CCDC22  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 49,105,726
GRCh38 X 49,249,265
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_021311.2:g.18801G>A
NG_007392.1:g.20563C>T
NC_000023.11:g.49249265G>A
NC_000023.10:g.49105726G>A
More... 		06/01/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CCDC22
Accession:XM_005272599
Location:INTRON

Gene Symbol:CCDC22
Accession:NM_014008
Location:INTRON

Gene Symbol:CCDC22
Accession:XR_430506
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003438301 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CCDC22 CLINVAR
OMIM 300859 CLINVAR