Variant #0000549157 (NC_000012.11:g.76740808A>G, NM_024685.3:c.957T>C (BBS10))

Chromosome 12
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.76740808A>G
DNA change (hg38) g.76347028A>G
Published as BBS10(NM_024685.4):c.957T>C (p.V319=)
ISCN -
DB-ID BBS10_000105
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 2020-07-02 17:02:47 +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.*8861T>C r.(=) p.(=)
BBS10 NM_024685.3 -/. - c.957T>C r.(?) p.(Val319=)


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