Variant #0001032520 (NC_000002.11:g.170344314A>G, NC_000002.11(NM_152384.2):c.209-2A>G (BBS5))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.170344314A>G
DNA change (hg38) -
Published as BBS5(NM_152384.2):c.209-2A>G, BBS5(NM_152384.3):c.209-2A>G
ISCN -
DB-ID BBS5_000007 See all 8 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BBS5 NM_152384.2 +?/. - c.209-2A>G r.spl? p.?


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