Variant #0000913262 (NC_000010.10:g.21112137A>T, NM_006393.2:c.1962T>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.21112137A>T
DNA change (hg38) -
Published as NEBL(NM_006393.3):c.1962T>A (p.N654K)
ISCN -
DB-ID C10orf113_000076
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) 0.05595 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.*302615T>A r.(=) p.(=)
NEBL NM_006393.2 -/. - c.1962T>A r.(?) p.(Asn654Lys)


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