RGD:11661594 Rat Genome Database

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Variant: RGD:11661594 -  Homo sapiens

RGD ID: 11661594
RS ID: rs886054731
ClinVar ID: CV282134
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLF11  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 10,193,935
GRCh38 2 10,053,808
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_017199.1:g.15254C>G
NC_000002.12:g.10053808C>G
NC_000002.11:g.10193935C>G
NM_001177716.2:c.*1301C>G
More... 		06/14/2016 3 prime utr variant uncertain significance Diabetes mellitus MODY type 7; MODY KLF11 related; MODY type 7
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:KLF11
Accession:XM_047446025
Location:3UTRS;EXON

Gene Symbol:KLF11
Accession:NM_001177716
Location:3UTRS;EXON

Gene Symbol:KLF11
Accession:NM_003597
Location:3UTRS;EXON

Gene Symbol:KLF11
Accession:NM_001177718
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000377927 CLINVAR
dbSNP (RS) rs886054731 CLINVAR
MedGen C1864839 CLINVAR
NCBI Gene KLF11 CLINVAR
OMIM 603301 CLINVAR
  610508 CLINVAR