Variant #0000322058 (NC_000011.9:g.8948487C>T, NM_020642.3:c.*7460C>T (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.8948487C>T
DNA change (hg38) g.8926940C>T
Published as C11orf16(NM_020643.2):c.559G>A (p.(Ala187Thr))
ISCN -
DB-ID C11orf16_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) 0 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKIP1 NM_020642.3 ?/. - c.*7460C>T r.(=) p.(=)
C11orf16 NM_020643.2 ?/. - c.559G>A r.(?) p.(Ala187Thr)


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