RGD:8635164 Rat Genome Database

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Summary

Variant: RGD:8635164 - Homo sapiens

RGD ID:

8635164

ClinVar ID:

CV90386

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

TRA TRAV26-1

Reference Nucleotide:

Variant Nucleotide:

Position

Assembly	Chr	Position
GRCh37	14	22,591,997
GRCh38	14	22,124,039

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_000014.7:g.21661837G>A NC_000014.9:g.22124039G>A NC_000014.8:g.22591997G>A		not provided	Malignant melanoma, 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.