Variant #0000996442 (NC_000007.13:g.27224230_27224235dup, NM_018951.3:c.-10299_-10294dup (HOXA10))

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.27224230_27224235dup
DNA change (hg38) -
Published as HOXA11(NM_005523.5):c.540_545dupGGCGGC (p.(Ala181_Ala182dup))
ISCN -
DB-ID HOXA9_000014
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXA11 NM_005523.5 ?/. - c.540_545dup r.(?) p.(Ala182_Ala183dup)
HOXA10 NM_018951.3 ?/. - c.-10299_-10294dup r.(?) p.(=)
HOXA9 NM_152739.3 ?/. - c.-19148_-19143dup r.(?) p.(=)


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