RGD:8582660 Rat Genome Database

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Summary

Variant: RGD:8582660 - Homo sapiens

RGD ID:

8582660

ClinVar ID:

CV117213

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

COL4A2

Reference Nucleotide:

Variant Nucleotide:

Position

Assembly	Chr	Position
GRCh37	13	111,065,327
GRCh38	13	110,412,980

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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
NM_001846.2:c.181-11754A>C NG_032137.1:g.110697A>C NC_000013.11:g.110412980A>C NC_000013.10:g.111065327A>C		intron\|intron variant	uncertain significance	Lung cancer, somatic