RGD:401778463 Rat Genome Database

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Variant: RGD:401778463 -  Homo sapiens

RGD ID: 401778463
ClinVar ID: CV2709153
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TACR3  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 104,640,705
GRCh38 4 103,719,548
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.128A>T
NG_023344.1:g.5269A>T
NC_000004.12:g.103719548T>A
NC_000004.11:g.104640705T>A
More... 		05/03/2023 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TACR3
Accession:NM_001059
Location:EXON
Amino Acid Prediction: Q to L (nonsynonymous)
Amino Acid Position: 43
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MATLPAAETWIDGGGGVGADAVNLTASLAAGAATGAVETGWLLLLDQAGNLSSSPSALGLPVASPAPSQPWANLTNQFVQ
PSWRIALWSLAYGVVVAVAVLGNLIVIWIILAHKRMRTVTNYFLVNLAFSDASMAAFNTLVNFIYALHSEWYFGANYCRF
QNFFPITAVFASIYSMTAIAVDRYMAIIDPLKPRLSATATKIVIGSIWILAFLLAFPQCLYSKTKVMPGRTLCFVQWPEG
PKQHFTYHIIVIILVYCFPLLIMGITYTIVGITLWGGEIPGDTCDKYHEQLKAKRKVVKMMIIVVMTFAICWLPYHIYFI
LTAIYQQLNRWKYIQQVYLASFWLAMSSTMYNPIIYCCLNKRFRAGFKRAFRWCPFIKVSSYDELELKTTRFHPNRQSSM
YTVTRMESMTVVFDPNDADTTRSSRKKRATPRDPSFNGCSRRNSKSASATSSFISSPYTSVDEYS*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003287071 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene TACR3 CLINVAR
OMIM 162332 CLINVAR