Variant #0000979579 (NC_000011.9:g.45925718G>A, NM_001080446.2:c.*2402C>T (C11orf94))

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.45925718G>A
DNA change (hg38) -
Published as MAPK8IP1(NM_005456.4):c.1666+6G>A
ISCN -
DB-ID C11orf94_000010
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) 1.0E-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 2024-04-19 20:27:30 +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     
C11orf94 NM_001080446.2 ?/. - c.*2402C>T r.(=) p.(=)
MAPK8IP1 NM_005456.3 ?/. - c.1666+6G>A r.(=) p.(=)


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