Variant #0000558493 (NC_000016.9:g.56531770A>G, NM_031885.3:c.1682T>C (BBS2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.56531770A>G
DNA change (hg38) g.56497858A>G
Published as BBS2(NM_031885.3):c.1682T>C (p.I561T), BBS2(NM_031885.5):c.1682T>C (p.(Ile561Thr))
ISCN -
DB-ID OGFOD1_000009 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) 5.0E-5 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 2024-04-19 20:27:30 +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.*21653A>G r.(=) p.(=)
BBS2 NM_031885.3 ?/. - c.1682T>C r.(?) p.(Ile561Thr)


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