Variant #0000600574 (NC_000005.9:g.172662300C>A, NM_004387.3:c.-214G>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.172662300C>A
DNA change (hg38) g.173235297C>A
Published as -
ISCN -
DB-ID NKX2-5_001346
Variant remarks rs909613811
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Liliana Dain
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2019-10-29 14:46:57 +01:00 (CET)
Date last edited 2021-09-09 14:48:34 +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 ?/. 1 c.-214G>T r.(?) p.(=)


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