Variant #0000947417 (NC_000002.11:g.176957721_176957726dup, NM_000523.3:c.103_108dup (HOXD13))

Chromosome 2
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.176957721_176957726dup
DNA change (hg38) -
Published as HOXD13(NM_000523.4):c.103_108dup (p.(Ala35_Ala36dup)), HOXD13(NM_000523.4):c.103_108dupGCGGCG (p.A35_A36dup)
ISCN -
DB-ID HOXD13_000029 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) 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXD13 NM_000523.3 ?/. - c.103_108dup r.(?) p.(Ala35_Ala36dup)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.