Variant #0000289157 (NC_000007.13:g.27239328_27239345del, NM_000522.4:c.360_377del (HOXA13))

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.27239328_27239345del
DNA change (hg38) g.27199709_27199726del
Published as HOXA13(NM_000522.5):c.360_377delTGCCGCGGCTGCCGCTGC (p.A128_A133del)
ISCN -
DB-ID HOXA13_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXA13 NM_000522.4 ?/. - c.360_377del r.(?) p.(Ala128_Ala133del)


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