Variant #0000611032 (NC_000007.13:g.27150191C>T, NM_002141.4:c.*18653G>A (HOXA4))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27150191C>T
DNA change (hg38) g.27110572C>T
Published as HOXA3(NM_153631.3):c.69G>A (p.G23=)
ISCN -
DB-ID HOXA3_000007
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) 0.00029 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXA4 NM_002141.4 -/. - c.*18653G>A r.(=) p.(=)
HOXA3 NM_030661.4 -/. - c.69G>A r.(?) p.(Gly23=)


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