RGD:127316692 Rat Genome Database

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Variant: RGD:127316692 -  Homo sapiens

RGD ID: 127316692
RS ID: rs779988555
ClinVar ID: CV1149525
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: VAPB  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 57,016,031
GRCh38 20 58,440,975
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001195677.2:c.212-3102G>A
NM_004738.5:c.465G>A
LRG_656:g.56787G>A
NG_008073.2:g.56787G>A
More... 		02/15/2020 intron variant likely benign Adult proximal spinal muscular atrophy, autosomal dominant; Adult-onset proximal spinal muscular atrophy, autosomal dominant; FINKEL LATE-ADULT TYPE SMA; Spinal muscular atrophy, late-onset, finkel type
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:VAPB
Accession:NM_004738
Location:EXON
Amino Acid Prediction: K to K (synonymous)
Amino Acid Position: 155
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAKVEQVLSLEPQHELKFRGPFTDVVTTNLKLGNPTDRNVCFKVKTTAPRRYCVRPNSGIIDAGASINVSVMLQPFDYDP
NEKSKHKFMVQSMFAPTDTSDMEAVWKEAKPEDLMDSKLRCVFELPAENDKPHDVEINKIISTTASKTETPIVSKSLSSS
LDDTEVKKVMEECKRLQGEVQRLREENKQFKEEDGLRMRKTVQSNSPISALAPTGKEEGLSTRLLALVVLFFIVGVIIGK
IAL*

Gene Symbol:VAPB
Accession:NR_036633
Location:EXON;NON-CODING

Gene Symbol:VAPB
Accession:XR_001754433
Location:EXON;NON-CODING

Gene Symbol:VAPB
Accession:NM_001195677
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002254670 CLINVAR
dbSNP (RS) rs779988555 CLINVAR
MedGen C1837728 CLINVAR
NCBI Gene VAPB CLINVAR
OMIM 182980 CLINVAR
  605704 CLINVAR
  608627 CLINVAR