RGD:401753808 Rat Genome Database

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Variant: RGD:401753808 -  Homo sapiens

RGD ID: 401753808
ClinVar ID: CV2685065
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CCL7  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 17 32,598,219
GRCh38 17 34,271,200
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_006273.2:c.131C>G
NP_006264.2:p.Pro44Arg
NM_006273.4:c.131C>G
NC_000017.11:g.34271200C>G
More... 		04/18/2023 missense variant uncertain significance AllHighlyPenetrant

Gene Symbol:CCL7
Accession:NM_006273
Location:EXON
Amino Acid Prediction: P to R (nonsynonymous)
Amino Acid Position: 44
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKASAALLCLLLTAAAFSPQGLAQPVGINTSTTCCYRFINKKIRKQRLESYRRTTSSHCPREAVIFKTKLDKEICADPTQ
KWVQDFMKHLDKKTQTPKL*
.


Database
Acc Id
Source(s)
ClinVar RCV004289644 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CCL7 CLINVAR
OMIM 158106 CLINVAR