Variant #0000614959 (NC_000014.8:g.36988353_36988381del, NM_003317.3:c.188_216del (NKX2-1))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.36988353_36988381del
DNA change (hg38) g.36519148_36519176del
Published as NKX2-1(NM_001079668.2):c.278_306del (p.(Ala93GlyfsTer336))
ISCN -
DB-ID NKX2-1_000026
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-05 14:07:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SFTA3 NM_001101341.1 +?/. - c.-6017_-5989del r.(?) p.(=)
NKX2-1 NM_003317.3 +?/. - c.188_216del r.(?) p.(Ala63GlyfsTer336)


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