rs57897376 Rat Genome Database

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Variant: rs57897376 -  Homo sapiens

RGD ID: 150458680
RS ID: rs57897376
ClinVar ID: CV1235969
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ALAS2  LOC108663984  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 55,054,001
GRCh38 X 55,027,568
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001037968.4:c.57+183C>T
LRG_1163:g.8497C>T
NG_051542.1:g.3912G>A
NC_000023.11:g.55027568G>A
More... 		07/07/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ALAS2
Accession:NM_000032
Location:5UTRS;INTRON

Gene Symbol:ALAS2
Accession:NM_001037967
Location:5UTRS;INTRON

Gene Symbol:ALAS2
Accession:NM_001037968
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001648939 CLINVAR
dbSNP (RS) rs57897376 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ALAS2 CLINVAR
  LOC108663984 CLINVAR
OMIM 301300 CLINVAR