RGD:405062762 Rat Genome Database

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Variant: RGD:405062762 -  Homo sapiens

RGD ID: 405062762
ClinVar ID: CV3148442
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NEUROG3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 71,332,630
GRCh38 10 69,572,874
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_020999.4:c.170C>T
NG_021321.1:g.5581C>T
NC_000010.11:g.69572874G>A
NC_000010.10:g.71332630G>A
More... 		11/27/2023 missense variant uncertain significance none provided

Gene Symbol:NEUROG3
Accession:NM_020999
Location:EXON
Amino Acid Prediction: A to V (nonsynonymous)
Amino Acid Position: 57
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MTPQPSGAPTVQVTRETERSFPRASEDEVTCPTSAPPSPTRTRGNCAEAEEGGCRGVPRKLRARRGGRSRPKSELALSKQ
RRSRRKKANDRERNRMHNLNSALDALRGVLPTFPDDAKLTKIETLRFAHNYIWALTQTLRIADHSLYALEPPAPHCGELG
SPGGSPGDWGSLYSPVSQAGSLSPAASLEERPGLLGATFSACLSPGSLAFSDFL*

Gene Symbol:NEUROG3
Accession:XM_017016280
Location:EXON
Amino Acid Prediction: A to V (nonsynonymous)
Amino Acid Position: 57
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MTPQPSGAPTVQVTRETERSFPRASEDEVTCPTSAPPSPTRTRGNCAEAEEGGCRGVPRKLRARRGGRSRPKSELALSKQ
RRSRRKKANDRERNRMHNLNSALDALRGVLPTFPDDAKLTKIETLRFAHNYIWALTQTLRIADHSLYALEPPAPHCGELG
SPGGSPGDWGSLYSPVSQAGSLSPAASLEERPGLLGATFSACLSPGSLAFSDFL*
.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV003850398 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NEUROG3 CLINVAR
OMIM 604882 CLINVAR