RGD:28868775 Rat Genome Database

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Variant: RGD:28868775 -  Homo sapiens

RGD ID: 28868775
RS ID: rs144864808
ClinVar ID: CV870343
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GRIP1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 66,741,650
GRCh38 12 66,347,870
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001366722.1:c.*1149A>G
NM_001366723.1:c.*1149A>G
NG_021400.2:g.726396A>G
NM_021150.3:c.*1149A>G
More...
01/12/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:GRIP1
Accession:NM_001178074
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:NM_021150
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:XM_005268757
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:XM_005268754
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:XM_017019100
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:XM_017019098
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:NM_001366723
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:NM_001366724
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:NM_001366722
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:NM_001379351
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:NM_001379349
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:NM_001379348
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:NM_001379347
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:NM_001379345
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:NM_001379346
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:XM_047428622
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:XM_047428620
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:XM_047428619
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:XM_047428617
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:XM_047428621
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:XM_047428616
Location:3UTRS;EXON

Gene Symbol:GRIP1
Accession:XM_047428618
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001112718 CLINVAR
dbSNP (RS) rs144864808 CLINVAR
MedGen C4540040 CLINVAR
NCBI Gene GRIP1 CLINVAR
OMIM 604597 CLINVAR
  617667 CLINVAR