RGD:156364024 Rat Genome Database

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Variant: RGD:156364024 -  Homo sapiens

RGD ID: 156364024
ClinVar ID: CV2262757
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WNT10B  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 49,363,922
GRCh38 12 48,970,139
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003394.4:c.287C>A
NG_023347.1:g.6720C>A
NC_000012.12:g.48970139G>T
NC_000012.11:g.49363922G>T
More... 		02/10/2022 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:WNT10B
Accession:NM_003394
Location:EXON
Amino Acid Prediction: A to E (nonsynonymous)
Amino Acid Position: 96
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MLEEPRPRPPPSGLAGLLFLALCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSKRQLGLCLRNPDVTASALQGLHIAV
HECQHQLRDQRWNCSELEGGGRLPHHSAILKRGFRESAFSFSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRAK
LLQLQALSRGKSFPHSLPSPGPGSSPSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT
ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAIFIDTHNRNSGAFQPRLRPRRLSGELVYFEKSPDFCER
DPTMGSPGTRGRACNKTSRLLDGCGSLCCGRGHNVLRQTRVERCHCRFHWCCYVLCDECKVTEWVNVCK*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002813262 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene WNT10B CLINVAR
OMIM 601906 CLINVAR