chr13:49050981:T>C Detail (hg19) (RB1)

Information

Genome

Assembly Position
hg19 chr13:49,050,981-49,050,981
hg38 chr13:48,476,845-48,476,845 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000321.2:c.2663+2T>C
Ensemble ENST00000713857.1:c.2510+2T>C
ENST00000713858.1:c.2558+2T>C
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
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 2013-09-16 no assertion criteria provided retinoblastoma somatic Detail
Pathogenic 2021-11-03 criteria provided, single submitter not provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.500 retinoblastoma NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000321.3(RB1):c.2663+2T>C AND Retinoblastoma ClinVar Detail
NM_000321.3(RB1):c.2663+2T>C AND not provided ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs587778839 dbSNP
Genome
hg19
Position
chr13:49,050,981-49,050,981
Variant Type
snv
Reference Allele
T
Alternative Allele
C
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