Variant #0000974468 (NC_000002.11:g.170678478T>A, NM_014168.2:c.199A>T (METTL5))

Chromosome 2
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.170678478T>A
DNA change (hg38) -
Published as METTL5(NM_014168.4):c.199A>T (p.(Ile67Phe))
ISCN -
DB-ID METTL5_000008
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 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SSB NM_003142.4 ?/. - c.*10212T>A r.(=) p.(=)
METTL5 NM_014168.2 ?/. - c.199A>T r.(?) p.(Ile67Phe)


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