RGD:407450649 Rat Genome Database

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Variant: RGD:407450649 -  Homo sapiens

RGD ID: 407450649
ClinVar ID: CV3468455
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PTPN7  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 202,129,866
GRCh38 1 202,160,738
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001364877.2:c.-53+649C>T
NM_001199797.2:c.174+649C>T
NM_002832.3:c.70C>T
NC_000001.11:g.202160738G>A
More... 		03/25/2024 intron variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004662570 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene PTPN7 CLINVAR
OMIM 176889 CLINVAR