RGD:8650806 Rat Genome Database

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Variant: RGD:8650806 -  Homo sapiens

RGD ID: 8650806
ClinVar ID: CV127381
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC105375635  NECAB1  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 91,841,660
GRCh38 8 90,829,432
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000008.11:g.90829432A>T
NC_000008.10:g.91841660A>T
NM_022351.4:c.233+4607A>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:NECAB1
Accession:NM_022351
Location:INTRON

Gene Symbol:NECAB1
Accession:XM_011517213
Location:INTRON

Gene Symbol:LOC105375635
Accession:NR_188048
Location:INTRON;NON-CODING

Variant Samples