rs780975544 Rat Genome Database

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Variant: rs780975544 -  Homo sapiens

RGD ID: 151722040
RS ID: rs780975544
ClinVar ID: CV1421900
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TMEM126A  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 85,365,299
GRCh38 11 85,654,255
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001244735.2:c.69A>G
NG_017157.2:g.11337A>G
NC_000011.10:g.85654255A>G
NC_000011.9:g.85365299A>G
More... 		10/05/2022 synonymous variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:TMEM126A
Accession:NM_032273
Location:EXON

Gene Symbol:TMEM126A
Accession:NM_001244735
Location:EXON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001909884 CLINVAR
dbSNP (RS) rs780975544 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TMEM126A CLINVAR
OMIM 612988 CLINVAR