rs146391431 Rat Genome Database

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Variant: rs146391431 -  Homo sapiens

RGD ID: 150462793
RS ID: rs146391431
ClinVar ID: CV1263711
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SALL1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 51,184,890
GRCh38 16 51,150,979
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002968.3:c.76+187C>T
LRG_674:g.5294C>T
NG_007990.1:g.5294C>T
NC_000016.10:g.51150979G>A
More... 		11/16/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SALL1
Accession:NM_002968
Location:INTRON

Gene Symbol:SALL1
Accession:XM_047434442
Location:INTRON

Gene Symbol:SALL1
Accession:NM_001127892
Location:INTRON

Gene Symbol:SALL1
Accession:XM_047434444
Location:INTRON

Gene Symbol:SALL1
Accession:XM_047434443
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001682412 CLINVAR
dbSNP (RS) rs146391431 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SALL1 CLINVAR
OMIM 602218 CLINVAR