RGD:15197828 Rat Genome Database

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Variant: RGD:15197828 -  Homo sapiens

RGD ID: 15197828
RS ID: rs143557954
ClinVar ID: CV762161
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL36RN  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 113,820,092
GRCh38 2 113,062,515
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_012275.3:c.306G>A
NM_173170.1:c.306G>A
NG_031864.1:g.8878G>A
NC_000002.12:g.113062515G>A
More... 		03/06/2019 synonymous variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:IL36RN
Accession:NM_173170
Location:EXON
Amino Acid Prediction: R to R (synonymous)
Amino Acid Position: 102
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MVLSGALCFRMKDSALKVLYLHNNQLLAGGLHAGKVIKGEEISVVPNRWLDASLSPVILGVQGGSQCLSCGVGQEPTLTL
EPVNIMELYLGAKESKSFTFYRRDMGLTSSFESAAYPGWFLCTVPEADQPVRLTQLPENGGWNAPITDFYFQQCD*

Gene Symbol:IL36RN
Accession:NM_012275
Location:EXON
Amino Acid Prediction: R to R (synonymous)
Amino Acid Position: 102
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MVLSGALCFRMKDSALKVLYLHNNQLLAGGLHAGKVIKGEEISVVPNRWLDASLSPVILGVQGGSQCLSCGVGQEPTLTL
EPVNIMELYLGAKESKSFTFYRRDMGLTSSFESAAYPGWFLCTVPEADQPVRLTQLPENGGWNAPITDFYFQQCD*

Gene Symbol:IL36RN
Accession:XM_047443918
Location:EXON
Amino Acid Prediction: R to R (synonymous)
Amino Acid Position: 102
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MVLSGALCFRMKDSALKVLYLHNNQLLAGGLHAGKVIKGEEISVVPNRWLDASLSPVILGVQGGSQCLSCGVGQEPTLTL
EPVNIMELYLGAKESKSFTFYRRDMGLTSSFESAAYPGWFLCTVPEADQPVRLTQLPENGGWNAPITDFYFQQCD*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000934625 CLINVAR
dbSNP (RS) rs143557954 CLINVAR
MedGen C0343055 CLINVAR
NCBI Gene IL36RN CLINVAR
OMIM 605507 CLINVAR
  614204 CLINVAR
SNOMED CT 238612002 CLINVAR