Variant #0001053903 (NC_000011.9:g.61541572G>A, NM_013279.2:c.1222G>A (C11orf9))

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.61541572G>A
DNA change (hg38) -
Published as MYRF(NM_001127392.3):c.1249G>A (p.(Val417Ile))
ISCN -
DB-ID C11orf9_000063
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C11orf9 NM_001127392.3 ?/. - c.1249G>A r.(?) p.(Val417Ile)
C11orf9 NM_013279.2 ?/. - c.1222G>A r.(?) p.(Val408Ile)


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