Variant #0000611029 (NC_000007.13:g.27135314_27135325del, NM_005522.4:c.212_223del (HOXA1))

Chromosome 7
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.27135314_27135325del
DNA change (hg38) g.27095695_27095706del
Published as HOXA1(NM_005522.5):c.212_223delACCATCGCCACC (p.H71_H74del)
ISCN -
DB-ID HOXA1_000012
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) 4.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
HOXA1 NM_005522.4 ?/. - c.212_223del r.(?) p.(His71_His74del)
HOXA2 NM_006735.3 ?/. - c.*5025_*5036del r.(=) p.(=)


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