Variant #0000552538 (NC_000014.8:g.36986905_36986924dup, NM_003317.3:c.675_694dup (NKX2-1))

Chromosome 14
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.36986905_36986924dup
DNA change (hg38) g.36517700_36517719dup
Published as NKX2-1(NM_003317.4):c.675_694dupGCAGCAGCAACTGCAGCAGG (p.D232Gfs*40)
ISCN -
DB-ID NKX2-1_000019
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-05 14:06:04 +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.-4566_-4547dup r.(?) p.(=)
NKX2-1 NM_003317.3 +/. - c.675_694dup r.(?) p.(Asp232GlyfsTer40)


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