RGD:401923569 Rat Genome Database

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Pathways
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Variant: RGD:401923569 -  Homo sapiens

RGD ID: 401923569
ClinVar ID: CV2820073
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TACR3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 104,640,821
GRCh38 4 103,719,664
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.12C>T
NG_023344.1:g.5153C>T
NC_000004.12:g.103719664G>A
NC_000004.11:g.104640821G>A
More... 		08/01/2022 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TACR3
Accession:NM_001059
Location:EXON
Amino Acid Prediction: L to L (synonymous)
Amino Acid Position: 4
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MATLPAAETWIDGGGGVGADAVNLTASLAAGAATGAVETGWLQLLDQAGNLSSSPSALGLPVASPAPSQPWANLTNQFVQ
PSWRIALWSLAYGVVVAVAVLGNLIVIWIILAHKRMRTVTNYFLVNLAFSDASMAAFNTLVNFIYALHSEWYFGANYCRF
QNFFPITAVFASIYSMTAIAVDRYMAIIDPLKPRLSATATKIVIGSIWILAFLLAFPQCLYSKTKVMPGRTLCFVQWPEG
PKQHFTYHIIVIILVYCFPLLIMGITYTIVGITLWGGEIPGDTCDKYHEQLKAKRKVVKMMIIVVMTFAICWLPYHIYFI
LTAIYQQLNRWKYIQQVYLASFWLAMSSTMYNPIIYCCLNKRFRAGFKRAFRWCPFIKVSSYDELELKTTRFHPNRQSSM
YTVTRMESMTVVFDPNDADTTRSSRKKRATPRDPSFNGCSRRNSKSASATSSFISSPYTSVDEYS*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003435119 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TACR3 CLINVAR
OMIM 162332 CLINVAR