Variant #0001050880 (NC_000002.11:g.170681375C>A, NM_014168.2:c.-268G>T (METTL5))

Chromosome 2
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.170681375C>A
DNA change (hg38) -
Published as METTL5(NM_001293187.2):c.-44+3G>T
ISCN -
DB-ID METTL5_000010
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SSB NM_003142.4 -?/. - c.*13109C>A r.(=) p.(=)
METTL5 NM_014168.2 -?/. - c.-268G>T r.(?) p.(=)
UBR3 NM_172070.3 -?/. - c.-2643C>A r.(?) p.(=)


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