rs7701409 Rat Genome Database

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Variant: rs7701409 -  Homo sapiens

RGD ID: 150465428
RS ID: rs7701409
ClinVar ID: CV1277238
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LIFR  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 38,503,018
GRCh38 5 38,502,916
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.1438-117G>A
NM_001127671.2:c.1438-117G>A
NM_001364298.2:c.1438-117G>A
NM_002310.6:c.1438-117G>A
More... 		09/01/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LIFR
Accession:NM_001127671
Location:INTRON

Gene Symbol:LIFR
Accession:NM_002310
Location:INTRON

Gene Symbol:LIFR
Accession:XM_011514042
Location:INTRON

Gene Symbol:LIFR
Accession:XM_017009463
Location:INTRON

Gene Symbol:LIFR
Accession:NM_001364297
Location:INTRON

Gene Symbol:LIFR
Accession:XM_047417172
Location:INTRON

Gene Symbol:LIFR
Accession:NM_001364298
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001710532 CLINVAR
dbSNP (RS) rs7701409 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LIFR CLINVAR
OMIM 151443 CLINVAR