Variant #0000853829 (NC_000014.8:g.36988447G>C, NM_003317.3:c.116C>G (NKX2-1))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.36988447G>C
DNA change (hg38) -
Published as NKX2-1(NM_003317.4):c.116C>G (p.A39G)
ISCN -
DB-ID NKX2-1_000035
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 2022-05-09 15:40:45 +02:00 (CEST)
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.-6089C>G r.(?) p.(=)
NKX2-1 NM_003317.3 ?/. - c.116C>G r.(?) p.(Ala39Gly)


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