Variant #0000563156 (NC_000017.10:g.74729691G>A, NM_001080510.3:c.496G>A (METTL23))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74729691G>A
DNA change (hg38) g.76733609G>A
Published as METTL23(NM_001080510.3):c.496G>A (p.(Asp166Asn))
ISCN -
DB-ID METTL23_000004
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) 0.00596 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 2019-07-18 18:22:55 +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.496G>A r.(?) p.(Asp166Asn)
SRSF2 NM_001195427.1 -?/. - c.*1557C>T r.(=) p.(=)
MFSD11 NM_024311.3 -?/. - c.-4346G>A r.(?) p.(=)


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