RGD:155999910 Rat Genome Database

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Variant: RGD:155999910 -  Homo sapiens

RGD ID: 155999910
ClinVar ID: CV2396495
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC107986777  NPY  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 24,325,011
GRCh38 7 24,285,392
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000905.4:c.152C>A
NG_016148.1:g.6205C>A
NC_000007.14:g.24285392C>A
NC_000007.13:g.24325011C>A
More... 		09/15/2021 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:NPY
Accession:NM_000905
Location:EXON
Amino Acid Prediction: A to E (nonsynonymous)
Amino Acid Position: 51
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MLGNKRLGLSGLTLALSLLVCLGALAEAYPSKPDNPGEDAPAEDMARYYSELRHYINLITRQRYGKRSSPETLISDLLMR
ESTENVPRTRLEDPAMW*

Gene Symbol:LOC107986777
Accession:XR_007060256
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_007060254
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_007060258
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_001745123
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_001745122
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_001745127
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_007060255
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_001745132
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_007060257
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_001745124
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_001745121
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_001745130
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_001745125
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_001745128
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_001745131
Location:INTRON;NON-CODING

Gene Symbol:LOC107986777
Accession:XR_001745129
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004242205 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene NPY CLINVAR
OMIM 162640 CLINVAR