RGD:597674563 Rat Genome Database

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Variant: RGD:597674563 -  Homo sapiens

RGD ID: 597674563
ClinVar ID: CV3620842
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130063305  TNFSF9  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 6,534,976
GRCh38 19 6,534,965
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_003811.4:c.664G>A
NG_197722.1:g.201G>A
NC_000019.10:g.6534965G>A
NC_000019.9:g.6534976G>A
More... 		07/14/2024 missense variant uncertain significance AllHighlyPenetrant

Gene Symbol:TNFSF9
Accession:NM_003811
Location:EXON
Amino Acid Prediction: A to T (nonsynonymous)
Amino Acid Position: 222
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MEYASDASLDPEAPWPPAPRARACRVLPWALVAGLLLLLLLAAACAVFLACPWAVSGARASPGSAASPRLREGPELSPDD
PAGLLDLRQGMFAQLVAQNVLLIDGPLSWYSDPGLAGVSLTGGLSYKEDTKELVVAKAGVYYVFFQLELRRVVAGEGSGS
VSLALHLQPLRSAAGAAALALTVDLPPASSEARNSAFGFQGRLLHLSAGQRLGVHLHTEARTRHAWQLTQGATVLGLFRV
TPEIPAGLPSPRSE*
.


Database
Acc Id
Source(s)
ClinVar RCV004882879 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene LOC130063305 CLINVAR
  TNFSF9 CLINVAR
OMIM 606182 CLINVAR