Variant #0000611817 (NC_000009.11:g.111692143C>T, NM_003640.3:c.209G>A (IKBKAP))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.111692143C>T
DNA change (hg38) g.108929863C>T
Published as ELP1(NM_003640.3):c.209G>A (p.R70H), ELP1(NM_003640.5):c.209G>A (p.R70H)
ISCN -
DB-ID IKBKAP_000061 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) 0.00125 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IKBKAP NM_003640.3 -?/. - c.209G>A r.(?) p.(Arg70His)
FAM206A NM_017832.3 -?/. - c.-4624C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.