Variant #0000510309 (NC_000002.11:g.176981559A>G, NM_002148.3:c.-3A>G (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.176981559A>G
DNA change (hg38) g.176116831A>G
Published as HOXD10(NM_002148.4):c.-3A>G
ISCN -
DB-ID HOXD8_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) 3.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXD8 NM_001199746.1 -?/. - c.-13536A>G r.(?) p.(=)
HOXD10 NM_002148.3 -?/. - c.-3A>G r.(?) p.(=)
HOXD9 NM_014213.3 -?/. - c.-5938A>G r.(?) p.(=)
HOXD11 NM_021192.2 -?/. - c.*7689A>G r.(=) p.(=)


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