RGD:126913362 Rat Genome Database

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Variant: RGD:126913362 -  Homo sapiens

RGD ID: 126913362
RS ID: rs2125283019
ClinVar ID: CV1042485
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL17RC  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 9,972,632
GRCh38 3 9,930,948
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001367280.1:c.1342+5G>A
NM_001367278.1:c.1348+5G>A
NM_001203263.2:c.1387+5G>A
NM_001203265.2:c.1291+5G>A
More... 		08/23/2020 intron variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:IL17RC
Accession:XM_017007331
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007347
Location:INTRON

Gene Symbol:IL17RC
Accession:NM_001410711
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449078
Location:INTRON

Gene Symbol:IL17RC
Accession:NM_001203265
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449077
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007342
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007343
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007328
Location:INTRON

Gene Symbol:IL17RC
Accession:NM_001367278
Location:INTRON

Gene Symbol:IL17RC
Accession:NM_001367279
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449071
Location:INTRON

Gene Symbol:IL17RC
Accession:NM_032732
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007348
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_024453794
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449066
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007340
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007341
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007336
Location:INTRON

Gene Symbol:IL17RC
Accession:NM_001203263
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007330
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449070
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449072
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449075
Location:INTRON

Gene Symbol:IL17RC
Accession:NM_153460
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007337
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449080
Location:INTRON

Gene Symbol:IL17RC
Accession:NM_153461
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007338
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007333
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007335
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007334
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_024453793
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007327
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007326
Location:INTRON

Gene Symbol:IL17RC
Accession:NM_001367280
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449069
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007345
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449067
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449068
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449079
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007329
Location:INTRON

Gene Symbol:IL17RC
Accession:NM_001203264
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007339
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_017007332
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449073
Location:INTRON

Gene Symbol:IL17RC
Accession:XM_047449074
Location:INTRON

Gene Symbol:IL17RC
Accession:NR_037807
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001359146 CLINVAR
dbSNP (RS) rs2125283019 CLINVAR
MedGen C4225324 CLINVAR
NCBI Gene IL17RC CLINVAR
OMIM 610925 CLINVAR
  616445 CLINVAR