RGD:407523299 Rat Genome Database

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Variant: RGD:407523299 -  Homo sapiens

RGD ID: 407523299
ClinVar ID: CV3463137
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PCDHB15  PCDHB@  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 140,627,280
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_018935.4:c.2134C>T
NG_000017.2:g.215833C>T
NC_000005.10:g.141247712C>T
NC_000005.9:g.140627280C>T
More... 		03/25/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004653190 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene PCDHB15 CLINVAR
  PCDHB@ CLINVAR
OMIM 604967 CLINVAR
  606341 CLINVAR