Variant #0000924702 (NC_000007.13:g.27239279_27239280insCGCCTGGCC, NM_000522.4:c.421_422insAGGCGGGCC (HOXA13))

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.27239279_27239280insCGCCTGGCC
DNA change (hg38) -
Published as HOXA13(NM_000522.5):c.421_422insAGGCGGGCC (p.G140_P141insQAG)
ISCN -
DB-ID HOXA13_000016
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 2023-04-16 21:50:28 +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     
HOXA13 NM_000522.4 -?/. - c.421_422insAGGCGGGCC r.(?) p.(Gly140_Pro141insGlnAlaGly)


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