Variant #0000510230 (NC_000002.11:g.170350279A>G, NM_152384.2:c.551A>G (BBS5))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.170350279A>G
DNA change (hg38) g.169493769A>G
Published as BBS5(NM_152384.2):c.551A>G (p.N184S, p.(Asn184Ser)), BBS5(NM_152384.3):c.551A>G (p.N184S)
ISCN -
DB-ID BBS5_000035 See all 22 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) 0.00422 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
BBS5 NM_152384.2 -?/. - c.551A>G r.(?) p.(Asn184Ser)


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