rs34803021 Rat Genome Database

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Variant: rs34803021 -  Homo sapiens

RGD ID: 15167402
RS ID: rs34803021
ClinVar ID: CV704720
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: S1PR5  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 10,625,121
GRCh38 19 10,514,445
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000019.10:g.10514445G>A
NC_000019.9:g.10625121G>A
NM_001166215.1:c.567C>T
NP_001159687.1:p.Tyr189=
More... 		06/14/2018 synonymous variant benign none provided

Gene Symbol:S1PR5
Accession:NM_001166215
Location:EXON
Amino Acid Prediction: Y to Y (synonymous)
Amino Acid Position: 189
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MESGLLRPAPVSEVIVLHYNYTGKLRGARYQPGAGLRADAVVCLAVCAFIVLENLAVLLVLGRHPRFHAPMFLLLGSLTL
SDLLAGAAYAANILLSGPLTLKLSPALWFAREGGVFVALTASVLSLLAIALERSLTMARRGPAPVSSRGRTLAMAAAAWG
VSLLLGLLPALGWNCLGRLDACSTVLPLYAKAYVLFCVLAFVGILAAICALYARIYCQVRANARRLPARPGTAGTTSTRA
RRKPRSLALLRTLSVVLLAFVACWGPLFLLLLLDVACPARTCPVLLQADPFLGLAMANSLLNPIIYTLTNRDLRHALLRL
VCCGRHSCGRDPSGSQQSASAAEASGGLRRCLPPGLDGSFSGSERSSPQRDGLDTSGSTGSPGAPTAARTLVSEPAAD*

Gene Symbol:S1PR5
Accession:NM_030760
Location:EXON
Amino Acid Prediction: Y to Y (synonymous)
Amino Acid Position: 189
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MESGLLRPAPVSEVIVLHYNYTGKLRGARYQPGAGLRADAVVCLAVCAFIVLENLAVLLVLGRHPRFHAPMFLLLGSLTL
SDLLAGAAYAANILLSGPLTLKLSPALWFAREGGVFVALTASVLSLLAIALERSLTMARRGPAPVSSRGRTLAMAAAAWG
VSLLLGLLPALGWNCLGRLDACSTVLPLYAKAYVLFCVLAFVGILAAICALYARIYCQVRANARRLPARPGTAGTTSTRA
RRKPRSLALLRTLSVVLLAFVACWGPLFLLLLLDVACPARTCPVLLQADPFLGLAMANSLLNPIIYTLTNRDLRHALLRL
VCCGRHSCGRDPSGSQQSASAAEASGGLRRCLPPGLDGSFSGSERSSPQRDGLDTSGSTGSPGAPTAARTLVSEPAAD*
.
PMID:25741868   PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV000949050 CLINVAR
dbSNP (RS) rs34803021 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene S1PR5 CLINVAR
OMIM 605146 CLINVAR