Variant #0000613492 (NC_000011.9:g.62439569G>A, NM_024099.3:c.-544C>T (C11orf48))

Chromosome 11
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.62439569G>A
DNA change (hg38) g.62672097G>A
Published as -
ISCN -
DB-ID C11orf48_000005
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) 0.74468 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
METTL12 NM_001043229.1 -/. - c.*5046G>A r.(=) p.(=)
C11orf83 NM_001085372.2 -/. - c.265G>A r.(?) p.(Gly89Ser)
UBXN1 NM_015853.3 -/. - c.*4621C>T r.(=) p.(=)
C11orf48 NM_024099.3 -/. - c.-544C>T r.(?) p.(=)


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