Variant #0000521491 (NC_000004.11:g.123664150G>A, NM_001178007.1:c.1103G>A (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.123664150G>A
DNA change (hg38) g.122742995G>A
Published as BBS12(NM_001178007.2):c.1103G>A (p.R368H), BBS12(NM_152618.3):c.1103G>A (p.R368H)
ISCN -
DB-ID BBS12_000052 See all 2 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) 0.00115 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 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.1103G>A r.(?) p.(Arg368His)
BBS12 NM_152618.2 -/. - c.1103G>A r.(?) p.(Arg368His)


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