chr13:48954351:T>C Detail (hg19) (RB1)

Information

Genome

Assembly Position
hg19 chr13:48,954,351-48,954,351
hg38 chr13:48,380,215-48,380,215 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000321.2:c.1472T>C NP_000312.2:p.Leu491Pro
Ensemble ENST00000267163.6:c.1472T>C ENST00000267163.6:p.Leu491Pro
ENST00000650461.1:c.1472T>C ENST00000650461.1:p.Leu491Pro
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Uncertain significance
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 COSM6947508 COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Uncertain significance 2024-05-20 criteria provided, single submitter retinoblastoma germline Detail
Uncertain significance 2016-04-06 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.1472T>C (p.Leu491Pro) AND Retinoblastoma ClinVar Detail
NM_000321.3(RB1):c.1472T>C (p.Leu491Pro) AND not provided 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
rs587778848 dbSNP
Genome
hg19
Position
chr13:48,954,351-48,954,351
Variant Type
snv
Reference Allele
T
Alternative Allele
C
Genome browser