RGD:14731038 Rat Genome Database

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Summary

Variant: RGD:14731038 - Homo sapiens

RGD ID:

14731038

ClinVar ID:

CV671648

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

PALB2

Reference Nucleotide:

Variant Nucleotide:

Position

Assembly	Chr	Position
GRCh37	16	23,647,713

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Model

Annotation Click to see Annotation Detail View

ClinVar Data

HGVS Name(s)	Last Evaluated	Clinical Significance	Trait Synonyms
NM_024675.3:c.212-58A>C NC_000016.10:g.23636392T>G NC_000016.9:g.23647713T>G	06/15/2018	likely benign