Variant #0000563155 (NC_000017.10:g.74729111G>C, NM_001080510.3:c.136G>C (METTL23))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74729111G>C
DNA change (hg38) g.76733029G>C
Published as METTL23(NM_001206983.2):c.136G>C (p.E46Q)
ISCN -
DB-ID METTL23_000003
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) 0.00172 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 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.136G>C r.(?) p.(Glu46Gln)
SRSF2 NM_001195427.1 -/. - c.*2137C>G r.(=) p.(=)
MFSD11 NM_024311.3 -/. - c.-4926G>C r.(?) p.(=)


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