RGD:8581052 Rat Genome Database

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Summary

Variant: RGD:8581052 - Homo sapiens

RGD ID:

8581052

ClinVar ID:

CV115489

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

HCN1

Reference Nucleotide:

Variant Nucleotide:

Position

Assembly	Chr	Position
GRCh37	5	45,665,960
GRCh38	5	45,665,858

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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_000005.10:g.45665858C>A NC_000005.9:g.45665960C>A NM_021072.3:c.426-20250G>T		intron\|intron variant	uncertain significance	Lung cancer, somatic