Variant #0000558498 (NC_000016.9:g.56533830T>C, NC_000016.9(NM_031885.3):c.1398-11A>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.56533830T>C
DNA change (hg38) g.56499918T>C
Published as BBS2(NM_031885.5):c.1398-11A>G
ISCN -
DB-ID OGFOD1_000011
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 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.*23713T>C r.(=) p.(=)
BBS2 NM_031885.3 -?/. - c.1398-11A>G r.(=) p.(=)


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