RGD:8585194 Rat Genome Database

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Variant: RGD:8585194 -  Homo sapiens

RGD ID: 8585194
ClinVar ID: CV119775
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NECAB2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 84,020,208
GRCh38 16 83,986,603
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000016.10:g.83986603C>T
NC_000016.9:g.84020208C>T
NM_019065.2:c.460-3891C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:NECAB2
Accession:XM_047434240
Location:INTRON

Gene Symbol:NECAB2
Accession:NM_001329749
Location:INTRON

Gene Symbol:NECAB2
Accession:NM_019065
Location:INTRON

Gene Symbol:NECAB2
Accession:NM_001329748
Location:INTRON

Variant Samples