Variant #0000322270 (NC_000011.9:g.62433981C>T, NC_000011.9(NM_024099.3):c.538+1014G>A (C11orf48))

Chromosome 11
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.62433981C>T
DNA change (hg38) g.62666509C>T
Published as METTL12(NM_001043229.1):c.181C>T (p.(Gln61Ter))
ISCN -
DB-ID C11orf48_000001
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) 0.00229 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-30 17:08:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
METTL12 NM_001043229.1 ?/. - c.181C>T r.(?) p.(Gln61Ter)
C11orf83 NM_001085372.2 ?/. - c.-5237C>T r.(?) p.(=)
C11orf48 NM_024099.3 ?/. - c.538+1014G>A r.(=) p.(=)


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