Variant #0001029894 (NC_000005.9:g.172660056G>T, NM_004387.3:c.491C>A (NKX2-5))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.172660056G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID NKX2-5_000486 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1554093487
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-03-14 14:50:01 +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     
NKX2-5 NM_004387.3 +/. - c.491C>A r.(?) p.(Ser164Ter)


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