Variant #0000853508 (NC_000012.11:g.6638717_6638720del, NM_014865.3:c.3611_3614del (NCAPD2))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6638717_6638720del
DNA change (hg38) -
Published as NCAPD2(NM_014865.4):c.3611_3614delAGAG (p.E1204Afs*63)
ISCN -
DB-ID GAPDH_000006
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     
GAPDH NM_002046.4 +/. - c.-5042_-5039del r.(?) p.(=)
NCAPD2 NM_014865.3 +/. - c.3611_3614del r.(?) p.(Glu1204Alafs*63)


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