Variant #0000857875 (NC_000002.11:g.176983671_176983674del, NC_000002.11(NM_002148.3):c.746-11_746-8del (HOXD10))

Chromosome 2
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.176983671_176983674del
DNA change (hg38) -
Published as HOXD10(NM_002148.3):c.746-11_746-8delAATT
ISCN -
DB-ID HOXD8_000009
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 2022-05-09 15:51:19 +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     
HOXD8 NM_001199746.1 -?/. - c.-11424_-11421del r.(?) p.(=)
HOXD10 NM_002148.3 -?/. - c.746-11_746-8del r.(=) p.(=)
HOXD9 NM_014213.3 -?/. - c.-3826_-3823del r.(?) p.(=)


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