Variant #0000545075 (NC_000011.9:g.66278493C>G, NM_024649.4:c.57C>G (BBS1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66278493C>G
DNA change (hg38) g.66511022C>G
Published as BBS1(NM_024649.5):c.57C>G (p.A19=)
ISCN -
DB-ID BBS1_000112
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) 9.0E-5 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BBS1 NM_024649.4 -/. - c.57C>G r.(?) p.(Ala19=)
DPP3 NM_130443.2 -/. - c.*1771C>G r.(=) p.(=)


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