Variant #0000622367 (NC_000010.10:g.21177128G>C, NM_006393.2:c.267C>G (NEBL))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.21177128G>C
DNA change (hg38) g.20888199G>C
Published as NEBL(NM_006393.2):c.267C>G (p.Y89*), NEBL(NM_006393.3):c.267C>G (p.Y89*)
ISCN -
DB-ID C10orf113_000019 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) 0.00125 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.*237624C>G r.(=) p.(=)
NEBL NM_006393.2 -?/. - c.267C>G r.(?) p.(Tyr89Ter)


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