Variant #0000819450 (NC_000004.11:g.122768628T>C, BBS7(NM_176824.2):c.968A>G)

Individual ID 00388862
Chromosome 4
Allele Parent #1
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.122768628T>C
DNA change (hg38) g.121847473T>C
Published as BBS7, variant 1: c.968A>G/p.H323R, variant 2: c.968A>G/p.H323R
ISCN -
DB-ID BBS7_000091 See all 2 reported entries
Variant remarks solved, homozygous
Reference PubMed: Weisschuh 2020
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BBS7 NM_176824.2 +?/. - c.968A>G r.(?) p.(His323Arg)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000390105 DNA SEQ-NG blood RET8 targeted sequencing panel - see paper BBS7 1 LOVD