Variant #0000510308 (NC_000002.11:g.176964834C>A, NM_000523.3:c.*5376C>A (HOXD13))

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.176964834C>A
DNA change (hg38) g.176100106C>A
Published as HOXD12(NM_021193.3):c.305C>A (p.(Ala102Glu))
ISCN -
DB-ID HOXD12_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) 0.0006 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXD13 NM_000523.3 -?/. - c.*5376C>A r.(=) p.(=)
HOXD12 NM_021193.3 -?/. - c.305C>A r.(?) p.(Ala102Glu)


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