RGD:8581051 Rat Genome Database

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Summary

Variant: RGD:8581051 - Homo sapiens

RGD ID:

8581051

ClinVar ID:

CV115488

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

HCN1

Reference Nucleotide:

Variant Nucleotide:

Position

Assembly	Chr	Position
GRCh37	5	45,649,335
GRCh38	5	45,649,233

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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.45649233T>C NC_000005.9:g.45649335T>C NM_021072.3:c.426-3625A>G		intron\|intron variant	uncertain significance	Lung cancer, somatic