RGD:28910240 Rat Genome Database

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Variant: RGD:28910240 -  Homo sapiens

RGD ID: 28910240
RS ID: rs770665581
ClinVar ID: CV871124
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KL  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 13 33,638,789
GRCh38 13 33,064,652
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004795.4:c.*466A>T
NG_011485.1:g.53219A>T
NC_000013.11:g.33064652A>T
NC_000013.10:g.33638789A>T
More... 		01/13/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:KL
Accession:NM_004795
Location:3UTRS;EXON

Gene Symbol:KL
Accession:XM_006719895
Location:3UTRS;EXON

Gene Symbol:KL
Accession:XM_047430776
Location:INTRON

Gene Symbol:KL
Accession:XM_047430775
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001109000 CLINVAR
dbSNP (RS) rs770665581 CLINVAR
MedGen C4693864 CLINVAR
NCBI Gene KL CLINVAR
OMIM 604824 CLINVAR
  617994 CLINVAR