Variant #0000293126 (NC_000005.9:g.172662014G>A, NM_004387.3:c.73C>T (NKX2-5))

Chromosome 5
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.172662014G>A
DNA change (hg38) g.173235011G>A
Published as NKX2-5(NM_001166175.1):c.73C>T (p.(Arg25Cys)), NKX2-5(NM_001166175.2):c.73C>T (p.R25C), NKX2-5(NM_004387.4):c.73C>T (p.R25C)
ISCN -
DB-ID NKX2-5_000040 See all 27 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) 0.00336 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NKX2-5 NM_004387.3 -/. - c.73C>T r.(?) p.(Arg25Cys)


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