RGD:15138568 Rat Genome Database

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Variant: RGD:15138568 -  Homo sapiens

RGD ID: 15138568
RS ID: rs1580074737
ClinVar ID: CV787531
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LIFR  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 38,510,827
GRCh38 5 38,510,725
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001364297.2:c.737-7T>C
NM_001364298.2:c.737-7T>C
NC_000005.10:g.38510725A>G
NC_000005.9:g.38510827A>G
More... 		12/18/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LIFR
Accession:NM_001364297
Location:INTRON

Gene Symbol:LIFR
Accession:NM_001364298
Location:INTRON

Gene Symbol:LIFR
Accession:NM_002310
Location:INTRON

Gene Symbol:LIFR
Accession:XM_047417172
Location:INTRON

Gene Symbol:LIFR
Accession:NM_001127671
Location:INTRON

Gene Symbol:LIFR
Accession:XM_011514042
Location:INTRON

Gene Symbol:LIFR
Accession:XM_017009463
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000982493 CLINVAR
dbSNP (RS) rs1580074737 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LIFR CLINVAR
OMIM 151443 CLINVAR