Variant #0000894294 (NC_000017.10:g.74729179_74729182del, NM_001080510.3:c.204_207del (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.74729179_74729182del
DNA change (hg38) -
Published as METTL23(NM_001206983.3):c.204_207delGAAT (p.M68Ifs*9)
ISCN -
DB-ID METTL23_000008
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
METTL23 NM_001080510.3 +?/. - c.204_207del r.(?) p.(Met68Ilefs*9)
SRSF2 NM_001195427.1 +?/. - c.*2069_*2072del r.(=) p.(=)
MFSD11 NM_024311.3 +?/. - c.-4858_-4855del r.(?) p.(=)


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