rs201453175 Rat Genome Database

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Variant: rs201453175 -  Homo sapiens

RGD ID: 151797380
RS ID: rs201453175
ClinVar ID: CV1512846
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NEUROG3  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 71,332,274
GRCh38 10 69,572,518
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_020999.4:c.526G>C
NG_021321.1:g.5937G>C
NC_000010.11:g.69572518C>G
NC_000010.10:g.71332274C>G
More... 		07/17/2023 missense variant uncertain significance none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:NEUROG3
Accession:XM_017016280
Location:EXON
Amino Acid Prediction: V to L (nonsynonymous)
Amino Acid Position: 176
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MTPQPSGAPTVQVTRETERSFPRASEDEVTCPTSAPPSPTRTRGNCAEAEEGGCRGAPRKLRARRGGRSRPKSELALSKQ
RRSRRKKANDRERNRMHNLNSALDALRGVLPTFPDDAKLTKIETLRFAHNYIWALTQTLRIADHSLYALEPPAPHCGELG
SPGGSPGDWGSLYSPLSQAGSLSPAASLEERPGLLGATFSACLSPGSLAFSDFL*

Gene Symbol:NEUROG3
Accession:NM_020999
Location:EXON
Amino Acid Prediction: V to L (nonsynonymous)
Amino Acid Position: 176
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MTPQPSGAPTVQVTRETERSFPRASEDEVTCPTSAPPSPTRTRGNCAEAEEGGCRGAPRKLRARRGGRSRPKSELALSKQ
RRSRRKKANDRERNRMHNLNSALDALRGVLPTFPDDAKLTKIETLRFAHNYIWALTQTLRIADHSLYALEPPAPHCGELG
SPGGSPGDWGSLYSPLSQAGSLSPAASLEERPGLLGATFSACLSPGSLAFSDFL*
.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV001866810 CLINVAR
dbSNP (RS) rs201453175 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NEUROG3 CLINVAR
OMIM 604882 CLINVAR