Variant #0000807453 (NC_000016.9:g.56530895_56530896insCTG, NM_031885.3:c.1894_1895insAGC (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.56530895_56530896insCTG
DNA change (hg38) -
Published as BBS2(NM_031885.3):c.1894_1895insAGC (p.A631_R632insQ)
ISCN -
DB-ID OGFOD1_000031
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.*20778_*20779insCTG r.(=) p.(=)
BBS2 NM_031885.3 ?/. - c.1894_1895insAGC r.(?) p.(Ala631_Arg632insGln)


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