Variant #0000925448 (NC_000011.9:g.61539103G>A, NM_013279.2:c.845G>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.61539103G>A
DNA change (hg38) -
Published as MYRF(NM_001127392.3):c.872G>A (p.R291Q)
ISCN -
DB-ID C11orf9_000041
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +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     
C11orf9 NM_001127392.3 ?/. - c.872G>A r.(?) p.(Arg291Gln)
C11orf9 NM_013279.2 ?/. - c.845G>A r.(?) p.(Arg282Gln)


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