Variant #0001064249 (NC_000004.11:g.122747117A>C, NM_176824.2:c.2046T>G (BBS7))

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.122747117A>C
DNA change (hg38) -
Published as BBS7(NM_176824.3):c.2046T>G (p.(Phe682Leu))
ISCN -
DB-ID chr4_005239
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EXOSC9 NM_001034194.1 ?/. - c.*9106A>C r.(=) p.(=)
CCNA2 NM_001237.3 ?/. - c.-2334T>G r.(?) p.(=)
BBS7 NM_176824.2 ?/. - c.2046T>G r.(?) p.(Phe682Leu)


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