RGD:8688816 Rat Genome Database

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Variant: RGD:8688816 -  Homo sapiens

RGD ID: 8688816
RS ID: rs112418040
ClinVar ID: CV136533
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLF6  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 3,821,669
GRCh38 10 3,779,477
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012277.1:g.10805G>A
NC_000010.11:g.3779477C>T
NC_000010.10:g.3821669C>T
NM_001160124.2:c.*62G>A
More... 		3 prime utr variant|non-coding transcript variant not provided Hypotensive disorder

Variant Details
Variant Transcripts
Gene Symbol:KLF6
Accession:NM_001160124
Location:3UTRS;EXON

Gene Symbol:KLF6
Accession:NM_001300
Location:3UTRS;EXON

Gene Symbol:KLF6
Accession:NM_001160125
Location:3UTRS;EXON

Gene Symbol:KLF6
Accession:NR_027653
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000119253 CLINVAR
dbSNP (RS) rs112418040 CLINVAR
MedGen C0020649 CLINVAR
NCBI Gene KLF6 CLINVAR
OMIM 602053 CLINVAR