Variant #0000725848 (NC_000016.9:g.56519630dup, NM_031885.3:c.1931dup (BBS2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.56519630dup
DNA change (hg38) -
Published as BBS2(NM_031885.5):c.1931dupA (p.Y644*)
ISCN -
DB-ID OGFOD1_000007
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OGFOD1 NM_018233.3 +/. - c.*9513dup r.(?) p.(=)
BBS2 NM_031885.3 +/. - c.1931dup r.(?) p.(Tyr644Ter)


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