Variant #0000259230 (NC_000004.11:g.123664457C>T, NM_001178007.1:c.1410C>T (BBS12))

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.123664457C>T
DNA change (hg38) g.122743302C>T
Published as BBS12(NM_001178007.1):c.1410C>T (p.C470=), BBS12(NM_001178007.2):c.1410C>T (p.C470=)
ISCN -
DB-ID BBS12_000061 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) 0.18229 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
BBS12 NM_001178007.1 -/. - c.1410C>T r.(?) p.(Cys470=)
BBS12 NM_152618.2 -/. - c.1410C>T r.(?) p.(Cys470=)


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