Variant #0001034316 (NC_000004.11:g.123663854dup, NM_001178007.1:c.807dup (BBS12))

Chromosome 4
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.123663854dup
DNA change (hg38) -
Published as BBS12(NM_152618.3):c.807dup (p.(Glu270Argfs*42))
ISCN -
DB-ID BBS12_000170
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BBS12 NM_001178007.1 +?/. - c.807dup r.(?) p.(Glu270Argfs*42)
BBS12 NM_152618.2 +?/. - c.807dup r.(?) p.(Glu270Argfs*42)


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