Variant #0000558494 (NC_000016.9:g.56533694T>G, NM_031885.3:c.1523A>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.56533694T>G
DNA change (hg38) g.56499782T>G
Published as BBS2(NM_031885.3):c.1523A>C (p.Q508P), BBS2(NM_031885.5):c.1523A>C (p.Q508P, p.(Gln508Pro))
ISCN -
DB-ID OGFOD1_000010 See all 3 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) 0.00018 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 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OGFOD1 NM_018233.3 ?/. - c.*23577T>G r.(=) p.(=)
BBS2 NM_031885.3 ?/. - c.1523A>C r.(?) p.(Gln508Pro)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.