Variant #0000814174 (NC_000004.11:g.122776642A>G, BBS7(NM_176824.2):c.IVS6+2T>C)

Individual ID 00385350
Chromosome 4
Allele Parent #2
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.122776642A>G
DNA change (hg38) -
Published as [p.Q293E];[p.F372XfsX1]
ISCN -
DB-ID BBS7_000077 See all 4 reported entries
Variant remarks -
Reference PubMed: Deveault-2011
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BBS7 NM_176824.2 +?/. 6i c.IVS6+2T>C r.spl? p.?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000386579 DNA PCR - - BBS7 3 LOVD