Variant #0000959719 (NC_000014.8:g.36986926C>T, NM_003317.3:c.673G>A (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.36986926C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID NKX2-1_000042
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2139407155
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-02-01 18:26:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NKX2-1 NM_003317.3 +?/. - c.673G>A r.(?) p.(Ala225Thr)


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