RGD:8649707 Rat Genome Database

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Summary

Variant: RGD:8649707 - Homo sapiens

RGD ID:

8649707

ClinVar ID:

CV126281

Genic Status:

INTERGENIC

Type:

SNV (SO:0001483)

Reference Nucleotide:

Variant Nucleotide:

Position

Assembly	Chr	Position
GRCh37	8	106,310,097
GRCh38	8	105,297,869

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

ClinVar Data

HGVS Name(s)	Last Evaluated	Clinical Significance	Trait Synonyms
NC_000008.11:g.105297869T>C NC_000008.10:g.106310097T>C		uncertain significance	Lung cancer, somatic

Variant Details

Variant Samples

ClinVar GRCh37

ClinVar GRCh38

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.