Variant #0000322271 (NC_000011.9:g.62437278G>C, NC_000011.9(NM_024099.3):c.151-3C>G (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.62437278G>C
DNA change (hg38) g.62669806G>C
Published as C11orf48(NM_024099.3):c.151-3C>G (p.?)
ISCN -
DB-ID C11orf48_000002
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) 5.0E-5 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 17:08:16 +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.*2755G>C r.(=) p.(=)
C11orf83 NM_001085372.2 ?/. - c.-1940G>C r.(?) p.(=)
C11orf48 NM_024099.3 ?/. - c.151-3C>G r.spl? p.?


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