NM_020754.3(ARHGAP31):c.100+22259C>ARat Genome Database
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Variant : CV112319 (NM_020754.3(ARHGAP31):c.100+22259C>A) Homo sapiens

Symbol: CV112319
Name: NM_020754.3(ARHGAP31):c.100+22259C>A
RGD ID: 8577942
Condition: Lung cancer [RCV000092842]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARHGAP31   ARHGAP31-AS1  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NM_020754.3:c.100+22259C>A
NG_007665.2:g.27891C>A
NC_000003.12:g.119317263C>A
NC_000003.11:g.119036110C>A
Position
Human AssemblyChrPosition (strand)Source
GRCh383119,317,263 - 119,317,263CLINVAR
GRCh373119,036,110 - 119,036,110CLINVAR
Cytogenetic Map33q13.33CLINVAR
Trait Synonyms: Lung cancer, somatic




References - curated
1. RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations

Additional Information