Variant #0000974831 (NC_000002.11:g.190541743G>A, NM_144708.3:c.527G>A (ANKAR))

Chromosome 2
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.190541743G>A
DNA change (hg38) -
Published as ANKAR(NM_001378068.1):c.527G>A (p.(Arg176His))
ISCN -
DB-ID ANKAR_000002
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) 0.00026 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OSGEPL1 NM_022353.2 -?/. - c.*70180C>T r.(=) p.(=)
ANKAR NM_144708.3 -?/. - c.527G>A r.(?) p.(Arg176His)


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