RGD:21074196 Rat Genome Database

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Variant: RGD:21074196 -  Homo sapiens

RGD ID: 21074196
RS ID: rs1591595888
ClinVar ID: CV796865
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NECAP1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 8,242,528
GRCh38 12 8,089,932
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_015509.4:c.96-4C>T
NG_034155.1:g.12722C>T
NC_000012.12:g.8089932C>T
NC_000012.11:g.8242528C>T
 04/01/2018 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:NECAP1
Accession:NM_015509
Location:INTRON

Gene Symbol:NECAP1
Accession:NR_024260
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000994844 CLINVAR
dbSNP (RS) rs1591595888 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NECAP1 CLINVAR
OMIM 611623 CLINVAR