Variant #0000600539 (NC_000005.9:g.172662181C>T, NM_004387.3:c.-95G>A (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.172662181C>T
DNA change (hg38) g.173235178C>T
Published as -
ISCN -
DB-ID NKX2-5_001309
Variant remarks rs867501574
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency 0.00003
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.-95G>A r.(?) p.(=)


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