RGD:156007171 Rat Genome Database

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Variant: RGD:156007171 -  Homo sapiens

RGD ID: 156007171
ClinVar ID: CV2357861
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC129661096  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 123,680,119
GRCh38 3 123,961,272
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001308317.1:c.-499G>A
NM_022757.4:c.46G>A
NC_000003.12:g.123961272C>T
NC_000003.11:g.123680119C>T
More... 		10/27/2021 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004205142 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CCDC14 CLINVAR
OMIM 617147 CLINVAR