RGD:14734771 Rat Genome Database

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Summary

Variant: RGD:14734771 - Homo sapiens

RGD ID:

14734771

ClinVar ID:

CV671718

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

ANO5

Reference Nucleotide:

Variant Nucleotide:

Position

Assembly	Chr	Position
GRCh37	11	22,233,029

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
NM_213599.2:c.138+169G>A NC_000011.10:g.22211483G>A NC_000011.9:g.22233029G>A	06/14/2018	benign

Variant Details

Variant Transcripts

Gene Symbol:
Accession:
Location:	INTRON

Gene Symbol:	ANO5
Accession:	NM_001142649
Location:	INTRON

Gene Symbol:	ANO5
Accession:	NM_213599
Location:	INTRON

Gene Symbol:
Accession:
Location:	INTRON

Variant Samples

ClinVar GRCh37

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