Variant #0000994691 (NC_000005.9:g.139930460A>G, NM_017747.2:c.*11457A>G (ANKHD1))

Chromosome 5
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.139930460A>G
DNA change (hg38) -
Published as SRA1(NM_001035235.3):c.536T>C (p.(Ile179Thr))
ISCN -
DB-ID ANKHD1_000007
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) 0.00083 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 2024-08-28 13:16:32 +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     
EIF4EBP3 NM_003732.2 -?/. - c.*1613A>G r.(=) p.(=)
ANKHD1 NM_017747.2 -?/. - c.*11457A>G r.(=) p.(=)
ANKHD1-EIF4EBP3 NM_020690.5 -?/. - c.*1638A>G r.(=) p.(=)
SRA1 NR_045586.1 -?/. - n.1201T>C r.(?) -


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