chr13:49037894:T>C Detail (hg19) (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	chr13:49,037,894-49,037,894
hg38	chr13:48,463,758-48,463,758 View the variant detail on this assembly version.

HGVS

RB1

Type	Transcript	Protein
RefSeq	NM_000321.2:c.2134T>C	NP_000312.2:p.Cys712Arg
Ensemble	ENST00000713858.1:c.2107-1240T>C
	ENST00000713857.1:c.2134T>C	ENST00000713857.1:p.Cys712Arg
	ENST00000650461.1:c.2134T>C	ENST00000650461.1:p.Cys712Arg
	ENST00000267163.6:c.2134T>C	ENST00000267163.6:p.Cys712Arg
	ENST00000713856.1:c.2134T>C	ENST00000713856.1:p.Cys712Arg

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
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2024-05-20	criteria provided, multiple submitters, no conflicts	retinoblastoma	germline	Detail
Likely pathogenic	2018-03-09	criteria provided, single submitter	Hereditary cancer-predisposing syndrome	germline	Detail
Likely pathogenic	2019-11-21	criteria provided, single submitter	Hereditary 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.2134T>C (p.Cys712Arg) AND Retinoblastoma	ClinVar	Detail
NM_000321.3(RB1):c.2134T>C (p.Cys712Arg) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_000321.3(RB1):c.2134T>C (p.Cys712Arg) AND Hereditary retinoblastoma	ClinVar	Detail
NA	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs137853296 dbSNP
Genome: hg19
Position: chr13:49,037,894-49,037,894
Variant Type: snv
Reference Allele: T
Alternative Allele: C

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