RGD:155929832 Rat Genome Database

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Variant: RGD:155929832 -  Homo sapiens

RGD ID: 155929832
ClinVar ID: CV2369895
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TNFSF9  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 6,534,674
GRCh38 19 6,534,663
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_003811.4:c.362C>T
NC_000019.10:g.6534663C>T
NC_000019.9:g.6534674C>T
NM_003811.3:c.362C>T
More... 		01/07/2022 missense variant uncertain significance AllHighlyPenetrant

Gene Symbol:TNFSF9
Accession:NM_003811
Location:EXON
Amino Acid Prediction: T to M (nonsynonymous)
Amino Acid Position: 121
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MEYASDASLDPEAPWPPAPRARACRVLPWALVAGLLLLLLLAAACAVFLACPWAVSGARASPGSAASPRLREGPELSPDD
PAGLLDLRQGMFAQLVAQNVLLIDGPLSWYSDPGLAGVSLMGGLSYKEDTKELVVAKAGVYYVFFQLELRRVVAGEGSGS
VSLALHLQPLRSAAGAAALALTVDLPPASSEARNSAFGFQGRLLHLSAGQRLGVHLHTEARARHAWQLTQGATVLGLFRV
TPEIPAGLPSPRSE*
.


Database
Acc Id
Source(s)
ClinVar RCV004208366 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TNFSF9 CLINVAR
OMIM 606182 CLINVAR