Variant #0000281392 (NC_000007.13:g.27135332_27135340del, NM_005522.4:c.207_215del (HOXA1))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27135332_27135340del
DNA change (hg38) g.27095713_27095721del
Published as HOXA1(NM_005522.5):c.207_215delCCACCACCA (p.H70_H72del)
ISCN -
DB-ID HOXA1_000005
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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.207_215del r.(?) p.(His72_His74del)
HOXA2 NM_006735.3 -?/. - c.*5020_*5028del r.(=) p.(=)


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