Variant #0000999539 (NC_000011.9:g.8959369C>A, NM_020642.3:c.*18342C>A (AKIP1))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.8959369C>A
DNA change (hg38) -
Published as ASCL3(NM_020646.1):c.340G>T (p.(Ala114Ser))
ISCN -
DB-ID AKIP1_000001
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) 4.0E-5 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     
AKIP1 NM_020642.3 ?/. - c.*18342C>A r.(=) p.(=)
C11orf16 NM_020643.2 ?/. - c.-4940G>T r.(?) p.(=)
ASCL3 NM_020646.1 ?/. - c.340G>T r.(?) p.(Ala114Ser)


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