Variant #0000865510 (NC_000017.10:g.74729690_74729692del, NM_001080510.3:c.495_497del (METTL23))

Chromosome 17
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.74729690_74729692del
DNA change (hg38) -
Published as METTL23(NM_001206987.2):c.294_296delAGA (p.E98del)
ISCN -
DB-ID METTL23_000007
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +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.495_497del r.(?) p.(Glu165del)
SRSF2 NM_001195427.1 ?/. - c.*1560_*1562del r.(=) p.(=)
MFSD11 NM_024311.3 ?/. - c.-4347_-4345del r.(?) p.(=)


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