Variant #0000525236 (NC_000005.9:g.172662026C>G, NM_004387.3:c.61G>C (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.172662026C>G
DNA change (hg38) g.173235023C>G
Published as NKX2-5(NM_001166175.2):c.61G>C (p.E21Q), NKX2-5(NM_004387.3):c.61G>C (p.E21Q), NKX2-5(NM_004387.4):c.61G>C (p.(Glu21Gln))
ISCN -
DB-ID NKX2-5_000072 See all 8 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) 0.00107 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NKX2-5 NM_004387.3 -/. - c.61G>C r.(?) p.(Glu21Gln)


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