Variant #0000614957 (NC_000014.8:g.36987109_36987110del, NM_003317.3:c.491_492del (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.36987109_36987110del
DNA change (hg38) g.36517904_36517905del
Published as NKX2-1(NM_003317.4):c.491_492delGC (p.R164Pfs*244)
ISCN -
DB-ID NKX2-1_000024
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-05 14:06:44 +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.-4750_-4749del r.(?) p.(=)
NKX2-1 NM_003317.3 +?/. - c.491_492del r.(?) p.(Arg164ProfsTer244)


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