Variant #0000545111 (NC_000011.9:g.66293652T>G, NM_024649.4:c.1169T>G (BBS1))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.66293652T>G
DNA change (hg38) g.66526181T>G
Published as BBS1(NM_024649.4):c.1169T>G (p.M390R, p.(Met390Arg)), BBS1(NM_024649.5):c.1169T>G (p.M390R)
ISCN -
DB-ID BBS1_000001 See all 296 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) 0.00152 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +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.1169T>G r.(?) p.(Met390Arg)
ZDHHC24 NM_207340.1 +/. - c.*13348A>C r.(=) p.(=)


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