rs750201466 Rat Genome Database

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Variant: rs750201466 -  Homo sapiens

RGD ID: 152141740
RS ID: rs750201466
ClinVar ID: CV1583435
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TMEM126A  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 85,366,625
GRCh38 11 85,655,581
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_032273.4:c.281-13A>C
NM_001244735.2:c.71-13A>C
NG_017157.2:g.12663A>C
NC_000011.10:g.85655581A>C
More... 		09/30/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TMEM126A
Accession:NM_001244735
Location:INTRON

Gene Symbol:TMEM126A
Accession:NM_032273
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002120468 CLINVAR
dbSNP (RS) rs750201466 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TMEM126A CLINVAR
OMIM 612988 CLINVAR