chr13:48376917:G>A Detail (hg38) (RB1)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr13:48,951,053-48,951,053 View the variant detail on this assembly version.
hg38	chr13:48,376,917-48,376,917

HGVS

RB1

Type	Transcript	Protein
RefSeq	NM_000321.2:c.1216-1G>A
Ensemble	ENST00000650461.1:c.1216-1G>A
	ENST00000267163.6:c.1216-1G>A
	ENST00000713856.1:c.1216-1G>A
	ENST00000713857.1:c.1216-1G>A
	ENST00000713858.1:c.1216-1G>A

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic Likely pathogenic
Review star
Show details

Links

RB1

Type	Database	ID	Link
Gene	MIM	614041	OMIM
	HGNC	9884	HGNC
	Ensembl	ENSG00000139687	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM14211	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic Likely pathogenic	2024-05-20	criteria provided, multiple submitters, no conflicts	retinoblastoma	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.500	retinoblastoma	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000321.3(RB1):c.1216-1G>A AND Retinoblastoma	ClinVar	Detail
NA	DisGeNET	Detail

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs587778831 dbSNP
Genome: hg38
Position: chr13:48,376,917-48,376,917
Variant Type: snv
Reference Allele: G
Alternative Allele: A

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