Variant #0000545074 (NC_000011.9:g.66278475C>A, NC_000011.9(NM_024649.4):c.48-9C>A (BBS1))

Chromosome 11
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.66278475C>A
DNA change (hg38) g.66511004C>A
Published as BBS1(NM_024649.5):c.48-9C>A
ISCN -
DB-ID BBS1_000111
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) 2.0E-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.48-9C>A r.(=) p.(=)
DPP3 NM_130443.2 ?/. - c.*1753C>A r.(=) p.(=)


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