Variant #0000521430 (NC_000004.11:g.122750143dup, NC_000004.11(NM_176824.2):c.1677-258dup (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.122750143dup
DNA change (hg38) g.121828988dup
Published as BBS7(NM_176824.3):c.1677-258dupT
ISCN -
DB-ID CCNA2_000006
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EXOSC9 NM_001034194.1 -/. - c.*12132dup r.(?) p.(=)
CCNA2 NM_001237.3 -/. - c.-5358dup r.(?) p.(=)
BBS7 NM_176824.2 -/. - c.1677-258dup r.(=) p.(=)


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