Variant #0000300007 (NC_000010.10:g.21157621G>T, NM_006393.2:c.656C>A (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.21157621G>T
DNA change (hg38) g.20868692G>T
Published as NEBL(NM_006393.2):c.656C>A (p.A219D)
ISCN -
DB-ID NEBL_000020 See all 3 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) 0.0195 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +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     
C10orf113 NM_001010896.2 -/. - c.*257131C>A r.(=) p.(=)
NEBL NM_006393.2 -/. - c.656C>A r.(?) p.(Ala219Asp)


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