Variant #0000337066 (NC_000004.11:g.122749436G>T, NC_000004.11(NM_176824.2):c.1891-12C>A (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.122749436G>T
DNA change (hg38) g.121828281G>T
Published as BBS7(NM_176824.2):c.1891-12C>A, BBS7(NM_176824.3):c.1891-12C>A
ISCN -
DB-ID BBS7_000007 See all 3 reported entries
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) 0.76938 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.*11425G>T r.(=) p.(=)
CCNA2 NM_001237.3 -/. - c.-4653C>A r.(?) p.(=)
BBS7 NM_176824.2 -/. - c.1891-12C>A r.(=) p.(=)


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