Variant #0000321721 (NC_000010.10:g.101295220_101295228del, NM_145285.2:c.837_845del (NKX2-3))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.101295220_101295228del
DNA change (hg38) g.99535463_99535471del
Published as NKX2-3(NM_145285.2):c.817_825del (p.(Ala276_Ala278del))
ISCN -
DB-ID NKX2-3_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
NKX2-3 NM_145285.2 ?/. - c.837_845del r.(?) p.(Ala284_Ala286del)


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