RGD:8587327 Rat Genome Database

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Summary

Variant: RGD:8587327 - Homo sapiens

RGD ID:

8587327

ClinVar ID:

CV121954

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

PTCHD1-AS

Reference Nucleotide:

Variant Nucleotide:

Position

Assembly	Chr	Position
GRCh37	X	22,366,215
GRCh38	X	22,348,098

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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_000023.11:g.22348098C>T NC_000023.10:g.22366215C>T NR_073010.1:n.511+41565G>A		intron\|intron variant	uncertain significance	Lung cancer, somatic