Variant #0000521494 (NC_000004.11:g.123664162_123664163del, NM_001178007.1:c.1115_1116del (BBS12))

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.123664162_123664163del
DNA change (hg38) g.122743007_122743008del
Published as BBS12(NM_001178007.1):c.1114_1115del (p.(Phe372Ter)), BBS12(NM_001178007.1):c.1115_1116delTT (p.F372*), BBS12(NM_001178007.2):c.1115_1116delTT (p....)
ISCN -
DB-ID BBS12_000008 See all 14 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
BBS12 NM_001178007.1 ?/. - c.1115_1116del r.(?) p.(Phe372Ter)
BBS12 NM_152618.2 ?/. - c.1115_1116del r.(?) p.(Phe372Ter)


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