Variant #0000805019 (NC_000011.9:g.134093812C>T, NM_015261.2:c.9G>A (NCAPD3))

Chromosome 11
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.134093812C>T
DNA change (hg38) -
Published as NCAPD3(NM_015261.2):c.9G>A (p.A3=)
ISCN -
DB-ID NCAPD3_000022
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) 0.0001 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
NCAPD3 NM_015261.2 -?/. - c.9G>A r.(?) p.(Ala3=)
VPS26B NM_052875.3 -?/. - c.-1205C>T r.(?) p.(=)


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