RGD:8602602 Rat Genome Database

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Variant: RGD:8602602 -  Homo sapiens

RGD ID: 8602602
RS ID: rs11558595
ClinVar ID: CV40508
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127829727  PPIB  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 64,454,311
GRCh38 15 64,162,112
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_10t1:c.178G>T
LRG_10:g.6044G>T
NG_012979.1:g.6044G>T
NC_000015.10:g.64162112C>A
More... 		02/17/2011 missense|missense variant not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:PPIB
Accession:NM_000942
Location:EXON
Amino Acid Prediction: V to L (nonsynonymous)
Amino Acid Position: 60
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MLRLSERNMKVLLAAALIAGSVFFLLLPGPSAADEKKKGPKVTVKVYFDLRIGDEDVGRLIFGLFGKTVPKTVDNFVALA
TGEKGFGYKNSKFHRVIKDFMIQGGDFTRGDGTGGKSIYGERFPDENFKLKHYGPGWVSMANAGKDTNGSQFFITTVKTA
WLDGKHVVFGKVLEGMEVVRKVESTKTDSRDKPLKDVIIADCGKIEVEKPFAIAKE*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000024542 CLINVAR
dbSNP (RS) rs11558595 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene PPIB CLINVAR
OMIM 123841 CLINVAR