RGD:15140599 Rat Genome Database

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Variant: RGD:15140599 -  Homo sapiens

RGD ID: 15140599
RS ID: rs1181816669
ClinVar ID: CV761396
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PTGS2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 186,645,968
GRCh38 1 186,676,836
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.186676836A>G
NP_000954.1:p.Tyr240=
NG_028206.2:g.8592T>C
NC_000001.10:g.186645968A>G
More... 		08/15/2018 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PTGS2
Accession:NM_000963
Location:EXON
Amino Acid Prediction: Y to Y (synonymous)
Amino Acid Position: 240
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MLARALLLCAVLALSHTANPCCSHPCQNRGVCMSVGFDQYKCDCTRTGFYGENCSTPEFLTRIKLFLKPTPNTVHYILTH
FKGFWNVVNNIPFLRNAIMSYVLTSRSHLIDSPPTYNADYGYKSWEAFSNLSYYTRALPPVPDDCPTPLGVKGKKQLPDS
NEIVEKLLLRRKFIPDPQGSNMMFAFFAQHFTHQFFKTDHKRGPAFTNGLGHGVDLNHIYGETLARQRKLRLFKDGKMKY
QIIDGEMYPPTVKDTQAEMIYPPQVPEHLRFAVGQEVFGLVPGLMMYATIWLREHNRVCDVLKQEHPEWGDEQLFQTSRL
ILIGETIKIVIEDYVQHLSGYHFKLKFDPELLFNKQFQYQNRIAAEFNTLYHWHPLLPDTFQIHDQKYNYQQFIYNNSIL
LEHGITQFVESFTRQIAGRVAGGRNVPPAVQKVSQASIDQSRQMKYQSFNEYRKRFMLKPYESFEELTGEKEMSAELEAL
YGDIDAVELYPALLVEKPRPDAIFGETMVEVGAPFSLKGLMGNVICSPAYWKPSTFGGEVGFQIINTASIQSLICNNVKG
CPFTSFSVPDPELIKTVTINASSSRSGLDDINPTVLLKERSTEL*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000943746 CLINVAR
dbSNP (RS) rs1181816669 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene PTGS2 CLINVAR
OMIM 600262 CLINVAR