Variant #0000549145 (NC_000012.11:g.76739646_76739647del, NM_024685.3:c.2119_2120del (BBS10))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.76739646_76739647del
DNA change (hg38) g.76345866_76345867del
Published as BBS10(NM_024685.4):c.2119_2120delGT (p.V707*)
ISCN -
DB-ID BBS10_000099 See all 8 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) Retrieve
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 2020-07-02 17:02:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BBS10 NM_024685.3 +?/. - c.2119_2120del r.(?) p.(Val707Ter)


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