RGD:156413997 Rat Genome Database

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Variant: RGD:156413997 -  Homo sapiens

RGD ID: 156413997
ClinVar ID: CV1979224
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127460100  SLC25A32  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 104,427,103
GRCh38 8 103,414,875
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NP_110407.2:p.Val21=
NM_015420.6:c.-116G>C
NM_030780.5:c.63C>G
NG_047200.1:g.5461C>G
More... 		07/26/2022 non-coding transcript variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:SLC25A32
Accession:NM_030780
Location:EXON
Amino Acid Prediction: V to V (synonymous)
Amino Acid Position: 21
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MTGQGQSASGSSAWSTVFRHVRYENLIAGVSGGVLSNLALHPLDLVKIRFAVSDGLELRPKYNGILHCLTTIWKLDGLRG
LYQGVTPNIWGAGLSWGLYFFFYNAIKSYKTEGRAERLEATEYLVSAAEAGAMTLCITNPLWVTKTRLMLQYDAVVNSPH
RQYKGMFDTLVKIYKYEGVRGLYKGFVPGLFGTSHGALQFMAYELLKLKYNQHINRLPEAQLSTVEYISVAALSKIFAVA
ATYPYQVVRARLQDQHMFYSGVIDVITKTWRKEGVGGFYKGIAPNLIRVTPACCITFVVYENVSHFLLDLREKRK*

Gene Symbol:SLC25A32
Accession:NR_102337
Location:EXON;NON-CODING

Gene Symbol:SLC25A32
Accession:NR_102338
Location:EXON;NON-CODING

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002609006 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC25A32 CLINVAR
OMIM 138480 CLINVAR