Variant #0000296488 (NC_000014.8:g.36986596C>A, NM_003317.3:c.1003G>T (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.36986596C>A
DNA change (hg38) g.36517391C>A
Published as NKX2-1(NM_003317.3):c.1003G>T (p.A335S), NKX2-1(NM_003317.4):c.1003G>T (p.A335S)
ISCN -
DB-ID NKX2-1_000002 See all 3 reported entries
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) 0.00089 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SFTA3 NM_001101341.1 -/. - c.-4238G>T r.(?) p.(=)
NKX2-1 NM_003317.3 -/. - c.1003G>T r.(?) p.(Ala335Ser)


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