Variant #0000849087 (NC_000002.11:g.177034130G>A, NM_006898.4:c.288G>A (HOXD3))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.177034130G>A
DNA change (hg38) -
Published as HOXD3(NM_006898.5):c.288G>A (p.G96=)
ISCN -
DB-ID HOXD3_000003
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) 0.01346 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:40:45 +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     
HOXD3 NM_006898.4 -/. - c.288G>A r.(?) p.(Gly96=)
HOXD4 NM_014621.2 -/. - c.*16460G>A r.(=) p.(=)


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