Variant #0000246242 (NC_000004.11:g.122747117A>G, NM_176824.2:c.2046T>C (BBS7))

Chromosome 4
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.122747117A>G
DNA change (hg38) g.121825962A>G
Published as BBS7(NM_176824.3):c.2046T>C (p.F682=)
ISCN -
DB-ID BBS7_000028
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EXOSC9 NM_001034194.1 -/. - c.*9106A>G r.(=) p.(=)
CCNA2 NM_001237.3 -/. - c.-2334T>C r.(?) p.(=)
BBS7 NM_176824.2 -/. - c.2046T>C r.(?) p.(Phe682=)


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