rs74127429 Rat Genome Database

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Variant: rs74127429 -  Homo sapiens

RGD ID: 150439347
RS ID: rs74127429
ClinVar ID: CV1266759
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: VPS45  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 150,063,871
GRCh38 1 150,091,777
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_033910.1:g.29485G>C
NM_001279354.2:c.997-160G>C
LRG_1170:g.29485G>C
NC_000001.11:g.150091777G>C
More... 		05/17/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:VPS45
Accession:NM_001279354
Location:INTRON

Gene Symbol:VPS45
Accession:NM_007259
Location:INTRON

Gene Symbol:VPS45
Accession:XM_024452791
Location:INTRON

Gene Symbol:VPS45
Accession:NM_001279353
Location:INTRON

Gene Symbol:VPS45
Accession:NR_103998
Location:INTRON;NON-CODING

Gene Symbol:VPS45
Accession:XR_007069452
Location:INTRON;NON-CODING

Gene Symbol:VPS45
Accession:XR_921734
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001690194 CLINVAR
dbSNP (RS) rs74127429 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene VPS45 CLINVAR
OMIM 610035 CLINVAR