RGD:15195269 Rat Genome Database

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Variant: RGD:15195269 -  Homo sapiens

RGD ID: 15195269
RS ID: rs375941892
ClinVar ID: CV766736
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TNFRSF10A  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 23,058,100
GRCh38 8 23,200,587
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003844.4:c.717T>C
NG_032107.1:g.29581T>C
NC_000008.11:g.23200587A>G
NC_000008.10:g.23058100A>G
More... 		06/29/2018 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TNFRSF10A
Accession:NM_003844
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 239
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAPPPARVHLGAFLAVTPNPGSAASGTEAAAATPSKVWGSSAGRIEPRGGGRGALPTSMGQHGPSARARAGRAPGPRPAR
EASPRLRVHKTFKFVVVGVLLQVVPSSAATIKLHDQSIGTQQWEHSPLGELCPPGSHRSEHPGACNRCTEGVGYTNASNN
LFACLPCTACKSDEEERSPCTTTRNTACQCKPGTFRNDNSAEMCRKCSRGCPRGMVKVKDCTPWSDIECVHKESGNGHNI
WVILVVTLVVPLLLVAVLIVCCCIGSGCGGDPKCMDRVCFWRLGLLRGPGAEDNAHNEILSNADSLSTFVSEQQMESQEP
ADLTGVTVQSPGEAQCLLGPAEAEGSQRRRLLVPANGADPTETLMLFFDKFANIVPFDSWDQLMRQLDLTKNEIDVVRAG
TAGPGDALYAMLMKWVNKTGRNASIHTLLDALERMEERHAREKIQDLLVDSGKFIYLEDGTGSAVSLE*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000933889 CLINVAR
dbSNP (RS) rs375941892 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene TNFRSF10A CLINVAR
OMIM 603611 CLINVAR