Variant #0001056196 (NC_000017.10:g.74729699del, NM_001080510.3:c.504del (METTL23))

Chromosome 17
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.74729699del
DNA change (hg38) -
Published as METTL23(NM_001080510.5):c.504del (p.(Glu169Asnfs*36))
ISCN -
DB-ID METTL23_000012
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 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     
METTL23 NM_001080510.3 +?/. - c.504del r.(?) p.(Glu169Asnfs*36)
SRSF2 NM_001195427.1 +?/. - c.*1549del r.(?) p.(=)
MFSD11 NM_024311.3 +?/. - c.-4338del r.(?) p.(=)


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