Variant #0000852472 (NC_000010.10:g.21177152dup, NC_000010.10(NM_006393.2):c.259-8dup (NEBL))

Chromosome 10
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.21177152dup
DNA change (hg38) -
Published as NEBL(NM_006393.2):c.259-8dupT
ISCN -
DB-ID C10orf113_000020 See all 2 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C10orf113 NM_001010896.2 -/. - c.*237608dup r.(?) p.(=)
NEBL NM_006393.2 -/. - c.259-8dup r.(=) p.(=)


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