RGD:28874973 Rat Genome Database

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Variant: RGD:28874973 -  Homo sapiens

RGD ID: 28874973
RS ID: rs1056465665
ClinVar ID: CV880789
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLF11  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 10,194,737
GRCh38 2 10,054,610
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000002.11:g.10194737G>A
NM_003597.4:c.*2103G>A
NM_001177718.2:c.*2103G>A
NM_001177716.2:c.*2103G>A
More... 		04/27/2017 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:NM_003597
Location:3UTRS;EXON

Gene Symbol:KLF11
Accession:XM_047446025
Location:3UTRS;EXON

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001133682 CLINVAR
dbSNP (RS) rs1056465665 CLINVAR
MedGen C1864839 CLINVAR
NCBI Gene KLF11 CLINVAR
OMIM 603301 CLINVAR
  610508 CLINVAR