Variant #0000977667 (NC_000007.13:g.27140863T>A, NM_006735.3:c.613A>T (HOXA2))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27140863T>A
DNA change (hg38) -
Published as HOXA2(NM_006735.4):c.613A>T (p.K205*)
ISCN -
DB-ID HOXA2_000004
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXA4 NM_002141.4 +?/. - c.*27981A>T r.(=) p.(=)
HOXA2 NM_006735.3 +?/. - c.613A>T r.(?) p.(Lys205*)
HOXA3 NM_030661.4 +?/. - c.*6671A>T r.(=) p.(=)


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