Variant #0000549162 (NC_000012.11:g.76741281_76741282del, NM_024685.3:c.488_489del (BBS10))

Chromosome 12
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.76741281_76741282del
DNA change (hg38) g.76347501_76347502del
Published as BBS10(NM_024685.4):c.488_489delGA (p.R163Nfs*4)
ISCN -
DB-ID BBS10_000108
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-02 17:03:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OSBPL8 NM_020841.4 +/. - c.*8392_*8393del r.(=) p.(=)
BBS10 NM_024685.3 +/. - c.488_489del r.(?) p.(Arg163AsnfsTer4)


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