chr13:48881497:AG> Detail (hg19) (RB1)

Information

Genome

Assembly Position
hg19 chr13:48,881,497-48,881,498
hg38 chr13:48,307,361-48,307,362 

HGVS

Type Transcript Protein
RefSeq NM_000321.2:c.219_220delAG NP_000312.2:p.Arg73SerfsTer36
Ensemble ENST00000267163.6:c.219_220delAG ENST00000267163.6:p.Arg73SerfsTer36
ENST00000646097.1:c.219_220delAG ENST00000646097.1:p.Arg73SerfsTer44
Summary

MGeND

Clinical significance not provided
Variant entry 2
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
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 COSM1942249 COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
not provided ileum not provided MGS000041
(TMGS000094) 		Hitoshi Nakagama National Cancer Center Japan
not provided descending colon not provided MGS000041
(TMGS000094) 		Hitoshi Nakagama National Cancer Center Japan
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.500 retinoblastoma NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
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
rs587778862 dbSNP
Genome
hg19
Position
chr13:48,881,497-48,881,498
Variant Type
snv
Reference Allele
AG
Alternative Allele
-
Genome browser