RGD:15103463 Rat Genome Database

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Variant: RGD:15103463 -  Homo sapiens

RGD ID: 15103463
RS ID: rs1218879121
ClinVar ID: CV775497
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: YME1L1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 27,437,979
GRCh38 10 27,149,050
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001253866.2:c.34-10C>T
NM_014263.4:c.34-10C>T
NM_139312.3:c.34-10C>T
NG_047122.1:g.11229C>T
More... 		07/11/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:YME1L1
Accession:NM_014263
Location:INTRON

Gene Symbol:YME1L1
Accession:NM_139312
Location:INTRON

Gene Symbol:YME1L1
Accession:NM_001253866
Location:INTRON

Gene Symbol:YME1L1
Accession:XM_011519300
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000937203 CLINVAR
dbSNP (RS) rs1218879121 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene YME1L1 CLINVAR
OMIM 607472 CLINVAR