RGD:14738780 Rat Genome Database

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Variant: RGD:14738780 -  Homo sapiens

RGD ID: 14738780
RS ID: rs78710909
ClinVar ID: CV658069
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC105373605  LOC122819150  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 127,864,922
GRCh38 2 127,107,346
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_012042.1:g.4943C>G
NC_000002.12:g.127107346G>C
NC_000002.11:g.127864922G>C
NM_139343.2:c.-403C>G
More... 		06/19/2018 benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LOC105373605
Accession:XR_923311
Location:EXON;NON-CODING

Gene Symbol:LOC105373605
Accession:XR_923310
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000839562 CLINVAR
dbSNP (RS) rs78710909 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BIN1 CLINVAR
  LOC122819150 CLINVAR
OMIM 601248 CLINVAR