RGD:156107381 Rat Genome Database

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Variant: RGD:156107381 -  Homo sapiens

RGD ID: 156107381
ClinVar ID: CV1992370
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WNT10B  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 49,359,985
GRCh38 12 48,966,202
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.1063G>A
NG_023347.1:g.10657G>A
NC_000012.12:g.48966202C>T
NC_000012.11:g.49359985C>T
More... 		10/03/2022 missense variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:WNT10B
Accession:NM_003394
Location:EXON
Amino Acid Prediction: V to M (nonsynonymous)
Amino Acid Position: 355
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MLEEPRPRPPPSGLAGLLFLALCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSKRQLGLCLRNPDVTASALQGLHIAV
HECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESAFSFSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRAK
LLQLQALSRGKSFPHSLPSPGPGSSPSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT
ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAIFIDTHNRNSGAFQPRLRPRRLSGELVYFEKSPDFCER
DPTMGSPGTRGRACNKTSRLLDGCGSLCCGRGHNMLRQTRVERCHCRFHWCCYVLCDECKVTEWVNVCK*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002622440 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WNT10B CLINVAR
OMIM 601906 CLINVAR