RGD:151849039 Rat Genome Database

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Variant: RGD:151849039 -  Homo sapiens

RGD ID: 151849039
RS ID: rs1458405524
ClinVar ID: CV1439955
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TACR3  TACR3-AS1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 104,511,119
GRCh38 4 103,589,962
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001059.3:c.1118G>T
NG_023344.1:g.134855G>T
NC_000004.12:g.103589962C>A
NC_000004.11:g.104511119C>A
More... 		11/15/2021 missense variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:TACR3
Accession:NM_001059
Location:EXON
Amino Acid Prediction: W to L (nonsynonymous)
Amino Acid Position: 373
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MATLPAAETWIDGGGGVGADAVNLTASLAAGAATGAVETGWLQLLDQAGNLSSSPSALGLPVASPAPSQPWANLTNQFVQ
PSWRIALWSLAYGVVVAVAVLGNLIVIWIILAHKRMRTVTNYFLVNLAFSDASMAAFNTLVNFIYALHSEWYFGANYCRF
QNFFPITAVFASIYSMTAIAVDRYMAIIDPLKPRLSATATKIVIGSIWILAFLLAFPQCLYSKTKVMPGRTLCFVQWPEG
PKQHFTYHIIVIILVYCFPLLIMGITYTIVGITLWGGEIPGDTCDKYHEQLKAKRKVVKMMIIVVMTFAICWLPYHIYFI
LTAIYQQLNRWKYIQQVYLASFWLAMSSTMYNPIIYCCLNKRFRAGFKRAFRLCPFIKVSSYDELELKTTRFHPNRQSSM
YTVTRMESMTVVFDPNDADTTRSSRKKRATPRDPSFNGCSRRNSKSASATSSFISSPYTSVDEYS*

Gene Symbol:TACR3-AS1
Accession:NR_186501
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002016325 CLINVAR
dbSNP (RS) rs1458405524 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TACR3 CLINVAR
  TACR3-AS1 CLINVAR
OMIM 162332 CLINVAR