RGD:8585962 Rat Genome Database

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Summary

Variant: RGD:8585962 - Homo sapiens

RGD ID:

8585962

ClinVar ID:

CV120557

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

ZNF729

Reference Nucleotide:

Variant Nucleotide:

Position

Assembly	Chr	Position
GRCh37	19	22,483,593
GRCh38	19	22,300,791

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Model

Annotation Click to see Annotation Detail View

ClinVar Data

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NC_000019.10:g.22300791G>T NC_000019.9:g.22483593G>T NM_001242680.1:c.31-2967G>T		intron\|intron variant	uncertain significance	Lung cancer, somatic