Variant #0000258600 (NC_000016.9:g.56536740T>C, NC_000016.9(NM_031885.3):c.805-20A>G (BBS2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56536740T>C
DNA change (hg38) g.56502828T>C
Published as BBS2(NM_031885.3):c.805-20A>G (p.(=)), BBS2(NM_031885.5):c.805-20A>G
ISCN -
DB-ID BBS2_000078 See all 4 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) 0.00407 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +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.*26623T>C r.(=) p.(=)
BBS2 NM_031885.3 -?/. - c.805-20A>G r.(=) p.(=)


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