rs114694221 Rat Genome Database

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Variant: rs114694221 -  Homo sapiens

RGD ID: 150410364
RS ID: rs114694221
ClinVar ID: CV1176272
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CP  HPS3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 148,886,017
GRCh38 3 149,168,230
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_032383.5:c.2887+247A>G
NC_000003.12:g.149168230A>G
NC_000003.11:g.148886017A>G
LRG_563:g.43647A>G
More... 		07/10/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CP
Accession:XM_006713501
Location:INTRON

Gene Symbol:HPS3
Accession:XM_047449064
Location:INTRON

Gene Symbol:CP
Accession:XM_011512435
Location:INTRON

Gene Symbol:CP
Accession:XM_017005735
Location:INTRON

Gene Symbol:CP
Accession:NM_000096
Location:INTRON

Gene Symbol:CP
Accession:XM_006713499
Location:INTRON

Gene Symbol:CP
Accession:XM_006713500
Location:INTRON

Gene Symbol:CP
Accession:XM_017005734
Location:INTRON

Gene Symbol:HPS3
Accession:NM_032383
Location:INTRON

Gene Symbol:HPS3
Accession:XM_005247834
Location:INTRON

Gene Symbol:HPS3
Accession:NM_001308258
Location:INTRON

Gene Symbol:CP
Accession:NR_046371
Location:INTRON;NON-CODING

Gene Symbol:HPS3
Accession:XR_001740328
Location:INTRON;NON-CODING

Gene Symbol:CP
Accession:XR_427361
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001546600 CLINVAR
dbSNP (RS) rs114694221 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CP CLINVAR
  HPS3 CLINVAR
OMIM 117700 CLINVAR
  606118 CLINVAR