Variant #0000277981 (NC_000009.11:g.111692163G>A, NM_003640.3:c.189C>T (IKBKAP))

Chromosome 9
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.111692163G>A
DNA change (hg38) g.108929883G>A
Published as ELP1(NM_003640.5):c.189C>T (p.L63=)
ISCN -
DB-ID IKBKAP_000020
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) 0.01816 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 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     
IKBKAP NM_003640.3 -/. - c.189C>T r.(?) p.(Leu63=)
FAM206A NM_017832.3 -/. - c.-4604G>A r.(?) p.(=)


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