RGD:407488707 Rat Genome Database

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Variant: RGD:407488707 -  Homo sapiens

RGD ID: 407488707
ClinVar ID: CV3487396
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARPC4-TTLL3  LOC129936138  TTLL3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 9,852,015
GRCh38 3 9,810,331
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001366051.2:c.-105G>A
NM_001387446.1:c.-105G>A
NM_001387447.1:c.-105G>A
NM_001387449.1:c.-105G>A
More...
05/14/2024 5 prime utr variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004682790 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ARPC4-TTLL3 CLINVAR
  LOC129936138 CLINVAR
  TTLL3 CLINVAR
OMIM 619195 CLINVAR