Variant #0000677474 (NC_000005.9:g.172662014G>A, NM_004387.3:c.73C>T (NKX2-5))

Chromosome 5
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.172662014G>A
DNA change (hg38) -
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




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)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.