RGD:28897617 Rat Genome Database

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Variant: RGD:28897617 -  Homo sapiens

RGD ID: 28897617
RS ID: rs1906814777
ClinVar ID: CV877174
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127886409  SLC6A4  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 28,549,931
GRCh38 17 30,222,913
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000017.11:g.30222913G>T
NC_000017.10:g.28549931G>T
NM_001045.5:c.-218C>A
NM_001045.6:c.-218C>A
More... 		01/13/2018 5 prime utr variant uncertain significance behavioral disorder
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SLC6A4
Accession:NM_001045
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001123272 CLINVAR
dbSNP (RS) rs1906814777 CLINVAR
MedGen C0004930 CLINVAR
NCBI Gene SLC6A4 CLINVAR
OMIM 182138 CLINVAR