RGD:11661489 Rat Genome Database

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Variant: RGD:11661489 -  Homo sapiens

RGD ID: 11661489
RS ID: rs886057590
ClinVar ID: CV338336
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130067574  TNFRSF13C  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 42,322,307
GRCh38 22 41,926,303
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_184t1:c.165G>A
LRG_184:g.5515G>A
NG_007579.1:g.5515G>A
NC_000022.11:g.41926303C>T
More... 		01/13/2018 synonymous variant uncertain significance ANTIBODY DEFICIENCY DUE TO BAFFR DEFECT
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TNFRSF13C
Accession:NM_052945
Location:EXON
Amino Acid Prediction: T to T (synonymous)
Amino Acid Position: 55
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MRRGPRSLRGRDAPAPTPCVPAECFDLLVRHCVACGLLRTPRPKPAGASSPAPRTALQPQESVGAGAGEAALPLPGLLFG
APALLGLALVLALVLVGLVSWRRRQRRLRGASSAEAPDGDKDAPEPLDKVIILSPGISDATAPAWPPPGEDPGTTPPGHS
VPVPATELGSTELVTTKTAGPEQQ*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000376880 CLINVAR
dbSNP (RS) rs886057590 CLINVAR
MedGen C3150739 CLINVAR
NCBI Gene LOC130067574 CLINVAR
  TNFRSF13C CLINVAR
OMIM 606269 CLINVAR
  613494 CLINVAR