rs1355032514 Rat Genome Database

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Variant: rs1355032514 -  Homo sapiens

RGD ID: 150424013
RS ID: rs1355032514
ClinVar ID: CV1183781
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: SERAC1  
Reference Nucleotide: TCTCTCTCTCTCTCTCTCTCTATATA
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 6 158,564,361 - 158,564,387
GRCh38 6 158,143,329 - 158,143,355
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_032861.4:c.610-169_610-144del
NG_032889.1:g.29928_29953del
NC_000006.12:g.158143329_158143354del
NC_000006.11:g.158564361_158564386del
 08/11/2019 intron variant likely benign none provided

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Database
Acc Id
Source(s)
ClinVar RCV001556093 CLINVAR
dbSNP (RS) rs1355032514 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SERAC1 CLINVAR
OMIM 614725 CLINVAR