Variant #0000655813 (NC_000007.13:g.27135314_27135322del, NM_005522.4:c.215_223del (HOXA1))

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.27135314_27135322del
DNA change (hg38) g.27095695_27095703del
Published as HOXA1(NM_005522.4):c.215_223del (p.(His72_His74del)), HOXA1(NM_005522.4):c.215_223delATCGCCACC (p.H72_H74del)
ISCN -
DB-ID HOXA1_000002 See all 2 reported entries
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) 0.00152 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXA1 NM_005522.4 -/. - c.215_223del r.(?) p.(His72_His74del)
HOXA2 NM_006735.3 -/. - c.*5028_*5036del r.(=) p.(=)


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