Variant #0000558506 (NC_000016.9:g.56543857G>T, NC_000016.9(NM_031885.3):c.612+12C>A (BBS2))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56543857G>T
DNA change (hg38) g.56509945G>T
Published as BBS2(NM_031885.3):c.612+12C>A, BBS2(NM_031885.5):c.612+12C>A
ISCN -
DB-ID OGFOD1_000017 See all 2 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) 0.0041 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OGFOD1 NM_018233.3 -/. - c.*33740G>T r.(=) p.(=)
BBS2 NM_031885.3 -/. - c.612+12C>A r.(=) p.(=)


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