Variant #0000616827 (NC_000017.10:g.74729449del, NM_001080510.3:c.397del (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.74729449del
DNA change (hg38) g.76733367del
Published as METTL23(NM_001206987.2):c.196delC (p.Q66Kfs*18)
ISCN -
DB-ID METTL23_000005
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 2019-12-04 15:24:38 +01:00 (CET)
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.397del r.(?) p.(Gln133LysfsTer18)
SRSF2 NM_001195427.1 +?/. - c.*1799del r.(?) p.(=)
MFSD11 NM_024311.3 +?/. - c.-4588del r.(?) p.(=)


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