Variant #0000657874 (NC_000016.9:g.56536315T>A, NM_031885.3:c.994A>T (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.56536315T>A
DNA change (hg38) g.56502403T>A
Published as BBS2(NM_031885.3):c.994A>T (p.S332C)
ISCN -
DB-ID OGFOD1_000024
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) 1.0E-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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OGFOD1 NM_018233.3 ?/. - c.*26198T>A r.(=) p.(=)
BBS2 NM_031885.3 ?/. - c.994A>T r.(?) p.(Ser332Cys)


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