Variant #0000275498 (NC_000011.9:g.66276576G>A, NM_024649.4:c.-1555G>A (BBS1))

Chromosome 11
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.66276576G>A
DNA change (hg38) g.66509105G>A
Published as DPP3(NM_130443.3):c.2068G>A (p.E690K)
ISCN -
DB-ID DPP3_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) 0.07322 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
BBS1 NM_024649.4 -/. - c.-1555G>A r.(?) p.(=)
DPP3 NM_130443.2 -/. - c.2068G>A r.(?) p.(Glu690Lys)


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