Variant #0000950245 (NC_000014.8:g.36986822C>T, NM_003317.3:c.777G>A (NKX2-1))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36986822C>T
DNA change (hg38) -
Published as NKX2-1(NM_003317.4):c.777G>A (p.A259=)
ISCN -
DB-ID NKX2-1_000040
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) 4.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-11-27 17:35:39 +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     
SFTA3 NM_001101341.1 -/. - c.-4464G>A r.(?) p.(=)
NKX2-1 NM_003317.3 -/. - c.777G>A r.(?) p.(=)


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