Variant #0000890002 (NC_000011.9:g.61551849del, NM_013279.2:c.3172del (C11orf9))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.61551849del
DNA change (hg38) -
Published as MYRF(NM_001127392.3):c.3292delG (p.D1098Tfs*11)
ISCN -
DB-ID C11orf9_000039
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +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.3292del r.(?) p.(Asp1098Thrfs*11)
C11orf9 NM_013279.2 +?/. - c.3172del r.(?) p.(Asp1058Thrfs*11)
TMEM258 NM_014206.3 +?/. - c.*4870del r.(?) p.(=)


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